Occipital Lobe Epilepsy

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Results for "Occipital Lobe Epilepsy": 7 genes, 780 gene sets

Name
BOP Gene Polymicrogyria, bilateral occipital
ETL6 Gene Epilepsy, familial temporal lobe, 6
ETL2 Gene epilepsy, familial temporal lobe
ETL4 Gene epilepsy, occipitotemporal lobe, and migraine with aura
FMTLE Gene Epilepsy, familial mesial temporal lobe
KNDC1 Gene kinase non-catalytic C-lobe* domain (KIND) containing 1* The protein encoded by this gene is a Ras guanine nucleotide exchange factor that appears to negatively regulate dendritic growth in the brain. Knockdown of this gene in senescent umbilical vein endothelial cells partially reversed the senescence, showing that this gene could potentially be targeted by anti-aging therapies. [provided by RefSeq, Dec 2016]
ENFL2 Gene Epilepsy, nocturnal frontal lobe, type 2
Occipital Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Occipital Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Refractory Occipital Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Occipital Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Occipital Lobe Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Occipital Lobe in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
occipital lobe Gene Set From GAD Gene-Disease Associations genes associated with the disease occipital lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormal occipital lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal occipital lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
occipital lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue occipital lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
occipital lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue occipital lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
occipital lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue occipital lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
abnormal occipital lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal occipital lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Occipital lobe neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Occipital lobe neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Occipital lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Occipital lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Occipital lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Occipital lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Occipital lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Occipital lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Occipital lobe volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Occipital lobe volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant nocturnal frontal lobe epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, nocturnal frontal lobe, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, nocturnal frontal lobe, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, lateral temporal lobe, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, lateral temporal lobe, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, nocturnal frontal lobe, type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, nocturnal frontal lobe, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, nocturnal frontal lobe, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, nocturnal frontal lobe, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, nocturnal frontal lobe, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, nocturnal frontal lobe, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, Frontal Lobe Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Frontal Lobe from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Temporal Lobe Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Temporal Lobe from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Nocturnal Frontal Lobe, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 4 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Nocturnal Frontal Lobe, Type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Temporal Lobe, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Nocturnal Frontal Lobe, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 3 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Nocturnal Frontal Lobe, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 1 from the curated CTD Gene-Disease Associations dataset.
temporal lobe epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease temporal lobe epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 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.
epilepsy, temporal lobe Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, temporal lobe; sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, temporal lobe; Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; 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.
epilepsy, temporal lobe; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporal lobe epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease temporal lobe epilepsy 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.
nocturnal frontal lobe epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease nocturnal frontal lobe epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
confusion; epilepsy, temporal lobe Gene Set From GAD Gene-Disease Associations genes associated with the disease confusion; epilepsy, temporal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, frontal lobe Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, frontal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, frontal lobe; Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, frontal lobe; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporal lobe epilepsy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease temporal lobe epilepsy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Epilepsy, Frontal Lobe Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Frontal Lobe phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Temporal Lobe Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Temporal Lobe phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, familial temporal lobe, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, nocturnal frontal lobe, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, nocturnal frontal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, nocturnal frontal lobe, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, nocturnal frontal lobe, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, nocturnal frontal lobe, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, nocturnal frontal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, nocturnal frontal lobe, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, nocturnal frontal lobe, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, nocturnal frontal lobe, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, nocturnal frontal lobe, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Lateral Temporal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Lateral Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 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.
Refractory Frontal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Frontal Lobe Epilepsy 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.
Familial temporal lobe epilepsy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial temporal lobe epilepsy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Temporal lobe epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Temporal lobe epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Frontal lobe epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Frontal lobe epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant nocturnal frontal lobe epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Temporal lobe epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Temporal lobe epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nocturnal frontal lobe epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Frontal lobe epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Frontal lobe epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial temporal lobe epilepsy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial temporal lobe epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial temporal lobe epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial temporal lobe epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial temporal lobe epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial temporal lobe epilepsy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial temporal lobe epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nocturnal frontal lobe epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant nocturnal frontal lobe epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial temporal lobe epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial temporal lobe epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mesial temporal lobe epilepsy with hippocampal sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mesial temporal lobe epilepsy with hippocampal sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
epilepsy; myoclonic epilepsy, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; epilepsy, reflex Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; epilepsy, reflex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; epilepsy, tonic-clonic Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; epilepsy, tonic-clonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
occipital pole, left, lateral aspect Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in occipital pole, left, lateral aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
inferior occipital gyrus, right, superior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior occipital gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
occipital pole, left, superior aspect Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in occipital pole, left, superior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
superior occipital gyrus, left, superior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior occipital gyrus, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
inferior occipital gyrus, left, superior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior occipital gyrus, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
superior occipital gyrus, right, inferior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior occipital gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
superior occipital gyrus, right, superior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior occipital gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
superior occipital gyrus, left, inferior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior occipital gyrus, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
inferior occipital gyrus, left, inferior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior occipital gyrus, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
occipital pole, left, inferior aspect Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in occipital pole, left, inferior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
inferior occipital gyrus, right, inferior bank of gyrus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior occipital gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
occipital cortex Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in occipital cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
occipital neocortex_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in occipital neocortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
occipital neocortex_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in occipital neocortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
occipital neocortex_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in occipital neocortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
occipital neocortex_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in occipital neocortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
IZ in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner SZ in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer SZ in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
IZ in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
MZ in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner SZ in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer SZ in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SZ in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in medial temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
MZ in lateral temporal-occipital cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Cortical malformations, occipital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical malformations, occipital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polymicrogyria, bilateral occipital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polymicrogyria, bilateral occipital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Occipital horn syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Occipital horn syndrome from the curated CTD Gene-Disease Associations dataset.
Polymicrogyria, Bilateral Occipital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polymicrogyria, Bilateral Occipital from the curated CTD Gene-Disease Associations dataset.
occipital Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term occipital in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
occipital meningocele Gene Set From HPO Gene-Disease Associations genes associated with the occipital meningocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
occipital encephalocele Gene Set From HPO Gene-Disease Associations genes associated with the occipital encephalocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
occipital myelomeningocele Gene Set From HPO Gene-Disease Associations genes associated with the occipital myelomeningocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fusion of atlas and occipital bones Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fusion of atlas and occipital bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
occipital bone foramen Gene Set From MPO Gene-Phenotype Associations gene mutations causing the occipital bone foramen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent occipital bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent occipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal occipital bone morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal occipital bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small occipital bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small occipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
occipital horn syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the occipital horn syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
polymicrogyria, bilateral occipital Gene Set From OMIM Gene-Disease Associations genes associated with the polymicrogyria, bilateral occipital phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical malformations, occipital Gene Set From OMIM Gene-Disease Associations genes associated with the cortical malformations, occipital phenotype from the curated OMIM Gene-Disease Associations dataset.
occipital pole Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue occipital pole in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Occipital Myelomeningocele Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Occipital Myelomeningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Occipital Encephalocele Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Occipital Encephalocele 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.
Polymicrogyria, Bilateral Occipital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymicrogyria, Bilateral Occipital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cortical Malformations, Occipital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cortical Malformations, Occipital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Occipital Bone Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Occipital Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Occipital Slowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Occipital Slowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal occipital bone morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal occipital bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fusion of atlas and occipital bones Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fusion of atlas and occipital bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
occipital bone hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the occipital bone hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
occipital bossing Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the occipital bossing phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged occipital bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged occipital bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent occipital bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent occipital bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small occipital bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small occipital bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
occipital bone foramen Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the occipital bone foramen phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
broad occipital bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the broad occipital bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
flat occipital bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the flat occipital bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fusion of axis and occipital bones Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fusion of axis and occipital bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atlanto-occipital joint dislocation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atlanto-occipital joint dislocation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Occipital horn syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Occipital horn syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bilateral parasagittal parieto-occipital polymicrogyria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bilateral parasagittal parieto-occipital polymicrogyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transverse occipital sulcus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Transverse occipital sulcus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Occipital pole Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Occipital pole in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bilateral parasagittal parieto-occipital polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bilateral parasagittal parieto-occipital polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Occipital pachygyria and polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Occipital pachygyria and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Occipital encephalocele Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Occipital encephalocele phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal occipital encephalocele-skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal occipital encephalocele-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Occipital cortical area (total cortical area interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Occipital cortical area (total cortical area interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lateral occipital cortex volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lateral occipital cortex volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parietal Lobe Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Parietal Lobe in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Frontal Lobe Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Frontal Lobe in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Temporal Lobe Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Temporal Lobe in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
middle lobe syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease middle lobe syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
parietal lobe Gene Set From GAD Gene-Disease Associations genes associated with the disease parietal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontal lobe Gene Set From GAD Gene-Disease Associations genes associated with the disease frontal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporal lobe Gene Set From GAD Gene-Disease Associations genes associated with the disease temporal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lobe Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term lobe in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
olfactory lobe development Gene Set From GO Biological Process Annotations 2015 genes participating in the olfactory lobe development biological process from the curated GO Biological Process Annotations 2015 dataset.
lung lobe morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the lung lobe morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
lung lobe formation Gene Set From GO Biological Process Annotations 2015 genes participating in the lung lobe formation biological process from the curated GO Biological Process Annotations 2015 dataset.
Brain structure (temporal lobe volume) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Brain structure (temporal lobe volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
olfactory lobe agenesis Gene Set From HPO Gene-Disease Associations genes associated with the olfactory lobe agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontal lobe dementia Gene Set From HPO Gene-Disease Associations genes associated with the frontal lobe dementia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
FACT complex subunit Spt16, N-terminal lobe domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the FACT complex subunit Spt16, N-terminal lobe domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal prostate gland dorsolateral lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent right lung accessory lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent right lung accessory lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal right lung middle lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung middle lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pituitary intermediate lobe hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pituitary intermediate lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pituitary intermediate lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary intermediate lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pituitary intermediate lobe hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pituitary intermediate lobe hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lung lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lung lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
enlarged pituitary intermediate lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the enlarged pituitary intermediate lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal parietal lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal parietal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal prostate gland ventral lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland ventral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal right lung caudal lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung caudal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
prostate gland anterior lobe hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the prostate gland anterior lobe hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ear lobe hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ear lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal frontal lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal frontal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small prostate gland ventral lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small prostate gland ventral lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent prostate gland anterior lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent prostate gland anterior lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum anterior lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum anterior lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal temporal lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal temporal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal flocculonodular lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal flocculonodular lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small pituitary intermediate lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small pituitary intermediate lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
enlarged prostate gland anterior lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the enlarged prostate gland anterior lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum posterior lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small prostate gland dorsolateral lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small prostate gland dorsolateral lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small prostate gland anterior lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small prostate gland anterior lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small lung lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small lung lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent pituitary intermediate lobe Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent pituitary intermediate lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ear lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ear lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal prostate gland anterior lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland anterior lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal olfactory lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal right lung accessory lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung accessory lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired lung lobe morphogenesis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired lung lobe morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
H3K27ac_Brain Inferior Temporal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K4me3_Brain Mid Frontal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_Brain Mid Frontal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K9me3_Brain Mid Frontal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9me3_Brain Mid Frontal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K4me3_Brain Inferior Temporal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K9ac_Brain Mid Frontal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9ac_Brain Mid Frontal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K36me3_Brain Mid Frontal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_Brain Mid Frontal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K9me3_Brain Inferior Temporal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K4me1_Brain Inferior Temporal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me1_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K27me3_Brain Inferior Temporal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K4me1_Brain Mid Frontal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me1_Brain Mid Frontal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K27ac_Brain Mid Frontal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_Brain Mid Frontal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K27me3_Brain Mid Frontal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27me3_Brain Mid Frontal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K36me3_Brain Inferior Temporal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K9ac_Brain Inferior Temporal Lobe Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9ac_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
olfactory lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue olfactory lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
cerebral lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
temporal lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue temporal lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
anterior lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue anterior lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
frontal lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue frontal lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
cerebral lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
parietal lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue parietal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
temporal lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue temporal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
olfactory lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue olfactory lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
frontal lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue frontal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
cerebral lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
parietal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue parietal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
posterior lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
neural lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue neural lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
temporal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
breast lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue breast lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
antennal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue antennal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
frontal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue frontal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
olfactory lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue olfactory lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
anterior lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue anterior lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medial temporal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medial temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
optic lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue optic lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Dementia Of Frontal Lobe Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dementia Of Frontal Lobe Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neoplasm Of Temporal Lobe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neoplasm Of Temporal Lobe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Lobe Pleomorphic Xanthoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Lobe Pleomorphic Xanthoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Middle Lobe Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Middle Lobe Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neoplasm Of Frontal Lobe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neoplasm Of Frontal Lobe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Lobe Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontal Lobe Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Olfactory Lobe Agenesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Olfactory Lobe Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Frontal Lobe Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontal Lobe Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
absent right lung accessory lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent right lung accessory lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small lung lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small lung lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
temporal lobe atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal lobe atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small prostate gland anterior lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small prostate gland anterior lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prostate gland anterior lobe hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prostate gland anterior lobe hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prostate gland dorsolateral lobe hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prostate gland dorsolateral lobe hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal prostate gland anterior lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prostate gland anterior lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal prostate gland dorsolateral lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased prostate gland dorsolateral lobe weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased prostate gland dorsolateral lobe weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal pituitary intermediate lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pituitary intermediate lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pituitary intermediate lobe hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pituitary intermediate lobe hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired lung lobe morphogenesis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired lung lobe morphogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased prostate gland anterior lobe weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased prostate gland anterior lobe weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased prostate gland ventral lobe weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased prostate gland ventral lobe weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prostate gland ventral lobe hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prostate gland ventral lobe hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased prostate gland dorsolateral lobe weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased prostate gland dorsolateral lobe weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pituitary intermediate lobe hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pituitary intermediate lobe hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal prostate gland ventral lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prostate gland ventral lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent prostate gland anterior lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent prostate gland anterior lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased prostate gland ventral lobe weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased prostate gland ventral lobe weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prostate gland lateral lobe hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prostate gland lateral lobe hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small prostate gland ventral lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small prostate gland ventral lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent pituitary intermediate lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent pituitary intermediate lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal frontal lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal frontal lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal parietal lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal parietal lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged prostate gland dorsolateral lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged prostate gland dorsolateral lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged prostate gland ventral lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged prostate gland ventral lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged pituitary intermediate lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged pituitary intermediate lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small pituitary intermediate lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small pituitary intermediate lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small prostate gland dorsolateral lobe Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small prostate gland dorsolateral lobe phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal right lung middle lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal right lung middle lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal right lung accessory lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal right lung accessory lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal right lung caudal lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal right lung caudal lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum anterior lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum anterior lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ear lobe hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ear lobe hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased prostate gland anterior lobe weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased prostate gland anterior lobe weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal temporal lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lung lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lung lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal olfactory lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent lobe of thyroid gland Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent lobe of thyroid gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Lobe cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Lobe cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Middle lobe syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Middle lobe syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Parietal lobe neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Parietal lobe neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Temporal lobe neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Temporal lobe neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Frontal lobe neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Frontal lobe neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Temporal lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Temporal lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Frontal lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Frontal lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Olfactory lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Olfactory lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Anterior lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Anterior lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Frontal lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Frontal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Parietal lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Parietal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Olfactory lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Olfactory lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Temporal lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Temporal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Temporal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Anterior lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Anterior lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Frontal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Frontal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Antennal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Antennal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medial temporal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medial temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Olfactory lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Olfactory lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Parietal lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Parietal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Optic lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Optic lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Neural lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Neural lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Posterior lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medial lobe of mushroom body Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medial lobe of mushroom body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Prostate gland lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Prostate gland lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Breast lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Breast lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Vertical lobe of mushroom body Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Vertical lobe of mushroom body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Lobe size Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lobe size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lobe attachment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lobe attachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parietal lobe volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parietal lobe volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Temporal lobe volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Temporal lobe volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Behavioural changes in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Behavioural changes in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Memory dysfunction in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Memory dysfunction in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Language impairment in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Language impairment in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinsonism in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinsonism in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Medial temporal lobe substructure volumes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Medial temporal lobe substructure volumes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Brain structure (temporal lobe volume) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brain structure (temporal lobe volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lobe attachment (rater-scored or self-reported) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lobe attachment (rater-scored or self-reported) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lobe attachment (rater scored) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lobe attachment (rater scored) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epilepsy, progressive myoclonic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, partial, with variable foci Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, partial, with variable foci phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure 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.
Pyridoxal 5'-phosphate-dependent epilepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyridoxal 5'-phosphate-dependent epilepsy 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.
Epilepsy, progressive myoclonic 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive myoclonus epilepsy with ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive myoclonus epilepsy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant 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.
Focal epilepsy with speech disorder with or without mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, familial adult myoclonic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe myoclonic epilepsy in infancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe myoclonic epilepsy in infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia-focal epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyridoxine-dependent epilepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyridoxine-dependent epilepsy 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.
Epilepsy, Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Generalized from the curated CTD Gene-Disease Associations dataset.
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease 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.
EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.
Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Idiopathic Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Idiopathic Generalized 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.
Epilepsy, Female-Restricted, with Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Female-Restricted, with Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Cortical Dysplasia-Focal Epilepsy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cortical Dysplasia-Focal Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Progressive Myoclonic, 1b Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Progressive Myoclonic, 1b from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Rolandic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Rolandic from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, with Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, with Epilepsy from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Tonic-Clonic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Tonic-Clonic from the curated CTD Gene-Disease Associations dataset.
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Adult Myoclonic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 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.
Hyperekplexia and Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperekplexia and Epilepsy from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Partial, with Variable Foci Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Partial, with Variable Foci from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, HOT WATER, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, HOT WATER, 1 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.
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, HOT WATER, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, HOT WATER, 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Complex Partial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Complex Partial 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.
Epilepsy, Absence Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Absence from the curated CTD Gene-Disease Associations dataset.
Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy from the curated CTD Gene-Disease Associations dataset.
Pyridoxine-dependent epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyridoxine-dependent epilepsy 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.
Myoclonic Epilepsy, Juvenile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myoclonic Epilepsy, Juvenile from the curated CTD Gene-Disease Associations dataset.
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked 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.
Epilepsy, Partial, with Pericentral Spikes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Partial, with Pericentral Spikes from the curated CTD Gene-Disease Associations dataset.
Epilepsy Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Epilepsy in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
juvenile myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease juvenile myoclonic epilepsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
epilepsy syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease epilepsy syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
epilepsy syndrome Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease epilepsy syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
juvenile absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile absence 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 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.
complex partial epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease complex partial epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
epilepsy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epilepsy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
extratemporal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extratemporal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 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.
idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic generalized epilepsy 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.
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.
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.
partial motor epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial motor epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
focal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
epilepsy; fragile x syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; fragile x syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; anticoagulant complications Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; anticoagulant complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
drug toxicity; epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease drug toxicity; epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myoclonic epilepsy, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; malnutrition Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
drug eruptions; drug hypersensitivity; epilepsy; stevens-johnson syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease drug eruptions; drug hypersensitivity; epilepsy; stevens-johnson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; stevens-johnson syndrome; urticaria pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; stevens-johnson syndrome; urticaria pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; rett syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, tonic-clonic Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, tonic-clonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsies, partial; epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsies, partial; epilepsy 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.
childhood absence epilepsy. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood absence epilepsy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; epilepsy, generalized; Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; epilepsy, generalized; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
drug toxicity; epidermal necrolysis, toxic; epilepsy; stevens-johnson syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease drug toxicity; epidermal necrolysis, toxic; epilepsy; stevens-johnson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy and mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy and mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, complex partial Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, complex partial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
juvenile myoclonic epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease juvenile myoclonic epilepsy 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.
cysts; epilepsy; tuberous sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cysts; epilepsy; tuberous sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; hyperhomocysteinemia; recurrence; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; hyperhomocysteinemia; recurrence; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; thrombophilia 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.
epilepsy; hyperammonemia Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, juvenile myoclonic Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, juvenile myoclonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
drug-induced liver injury; epilepsy; hepatitis, toxic Gene Set From GAD Gene-Disease Associations genes associated with the disease drug-induced liver injury; epilepsy; hepatitis, toxic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; neurotoxicity syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; neurotoxicity syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
generalized epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease generalized epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; neurocysticercosis Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; neurocysticercosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, idiopathic generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, idiopathic generalized 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.
atrophy; epilepsy; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia 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.
epilepsy; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term epilepsy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Epilepsy (generalized) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Epilepsy (generalized) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Epilepsy (remission after treatment) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Epilepsy (remission after treatment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
focal epilepsy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease focal epilepsy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
epilepsy syndrome Gene Set From GWASdb SNP-Disease Associations genes associated with the disease epilepsy syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Epilepsy, Generalized Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Generalized phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Reflex Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Reflex phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Rolandic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Rolandic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Tonic-Clonic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Tonic-Clonic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Post-Traumatic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Post-Traumatic 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.
Epilepsy, Complex Partial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Complex Partial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myoclonic Epilepsy, Juvenile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myoclonic Epilepsy, Juvenile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Absence Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Absence phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, familial focal, with variable foci Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
?rolandic epilepsy, mental retardation, and speech dyspraxia Gene Set From OMIM Gene-Disease Associations genes associated with the ?rolandic epilepsy, mental retardation, and speech dyspraxia phenotype from the curated OMIM Gene-Disease Associations dataset.
polyhydramnios, megalencephaly, and symptomatic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the polyhydramnios, megalencephaly, and symptomatic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2b (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2b (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
generalized epilepsy and paroxysmal dyskinesia Gene Set From OMIM Gene-Disease Associations genes associated with the generalized epilepsy and paroxysmal dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.
centrotemporal epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the centrotemporal epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile myoclonic, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile myoclonic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, partial, with pericentral spikes Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, partial, with pericentral spikes phenotype from the curated OMIM Gene-Disease Associations dataset.
psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From OMIM Gene-Disease Associations genes associated with the psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, x-linked, with variable learning disabilities and behavior disorders Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, x-linked, with variable learning disabilities and behavior disorders phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, childhood absence, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} 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.
{myoclonic epilepsy, juvenile, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {myoclonic epilepsy, juvenile, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} 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.
?epilepsy, familial adult myoclonic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epilepsy, familial adult myoclonic, 5 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, juvenile myoclonic, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonic epilepsy, juvenile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, juvenile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, idiopathic generalized, susceptibility to 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 6} 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.
cortical dysplasia-focal epilepsy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cortical dysplasia-focal epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile myoclonic, susceptiblity to, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile myoclonic, susceptiblity to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, hot water, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, hot water, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, hot water, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, hot water, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, epilepsy, and diabetes syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, epilepsy, and diabetes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial adult myoclonic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial adult myoclonic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, pyridoxine-dependent Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, pyridoxine-dependent phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile myoclonic, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 8} 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.
epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, focal, with speech disorder and with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile myoclonic, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, juvenile myoclonic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, juvenile myoclonic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, myoclonic, familial adult, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, myoclonic, familial adult, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile absence, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile absence, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1a (unverricht and lundborg) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1a (unverricht and lundborg) phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1b Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2a (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2a (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
Myoclonic epilepsy of Lafora Gene Set From Reactome Pathways 2014 proteins participating in the Myoclonic epilepsy of Lafora pathway from the Reactome Pathways dataset.
Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Awakening Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Awakening Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Drug Resistant Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Drug Resistant Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Unexplained Death In Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay, Epilepsy, And Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay, Epilepsy, And Neonatal Diabetes 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.
Idiopathic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reflex Epilepsy, Audiogenic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reflex Epilepsy, Audiogenic 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.
Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Epilepsy, Juvenile, Susceptibility To, 4 (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Epilepsy, Juvenile, Susceptibility To, 4 (Disorder) 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.
Familial Progressive Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Post Stroke Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Post Stroke Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Onset Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Onset Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperekplexia And Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperekplexia And Epilepsy 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 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.
Epilepsy And Migraine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epilepsy And Migraine 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.
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.
Cryptogenic Tonic-Clonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptogenic Tonic-Clonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tonic-Clonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tonic-Clonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uncinate Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uncinate Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reflex Epilepsy, Photosensitive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reflex Epilepsy, Photosensitive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Convulsive Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Convulsive Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Impulsive Petit Mal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Impulsive Petit Mal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Myoclonic Epilepsy Of Janz Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Myoclonic Epilepsy Of Janz in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic-Atonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic-Atonic Epilepsy 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.
Idiopathic Partial Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Partial Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nocturnal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nocturnal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Northern Epilepsy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Northern Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cortical Dysplasia With Focal Epilepsy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cortical Dysplasia With Focal Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Febrile Infection Related Epilepsy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Febrile Infection Related Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Epilepsy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Epilepsy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gelastic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gelastic Epilepsy 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.
Secondary Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Startle Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Startle Epilepsy 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.
Generalized Epilepsy And Paroxysmal Dyskinesia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy And Paroxysmal Dyskinesia 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.
Amygdalo-Hippocampal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amygdalo-Hippocampal Epilepsy 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.
Digestive Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Digestive Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhinencephalic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhinencephalic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Menstrual Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Menstrual Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Infantile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Infantile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Childhood Epilepsy, Myoclonic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Epilepsy, Myoclonic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Juvenile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Juvenile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scn8A-Related Epilepsy With Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scn8A-Related Epilepsy With Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptogenic Partial Complex Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptogenic Partial Complex Epilepsy 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.
Immersion Related Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Immersion Related Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychomotor Retardation, Epilepsy, And Craniofacial Dysmorphism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychomotor Retardation, Epilepsy, And Craniofacial Dysmorphism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eating Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eating Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Myoclonic Epilepsy With Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Myoclonic Epilepsy With Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epilepsy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
sudden unexpected death in epilepsy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sudden unexpected death in epilepsy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Myoclonic epilepsy of Lafora Gene Set From Reactome Pathways 2024 proteins participating in the Myoclonic epilepsy of Lafora pathway from the Reactome Pathways 2024 dataset.
Epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Focal epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Focal epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Juvenile myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Juvenile myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic generalized epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 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.
pyridoxine-dependent epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease pyridoxine-dependent epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial focal epilepsy with variable foci Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial focal epilepsy with variable foci from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic generalized epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Focal epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extratemporal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extratemporal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation 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.
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.
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.
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.
Idiopathic generalized epilepsy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile myoclonic epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile myoclonic epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile absence epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile absence epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial motor epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial motor epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 8 northern epilepsy variant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 8 northern epilepsy variant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial adult myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complex partial epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex partial epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset vitamin B6-dependent epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset vitamin B6-dependent epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myoclonic-atonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myoclonic-atonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
pyridoxine-dependent epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease pyridoxine-dependent epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Photosensitive epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Photosensitive epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial adult myoclonic epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Reflex epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reflex epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial focal epilepsy with variable foci Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial focal epilepsy with variable foci in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cortical dysplasia-focal epilepsy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cortical dysplasia-focal epilepsy syndrome 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.
polyhydramnios, megalencephaly, and symptomatic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease polyhydramnios, megalencephaly, and symptomatic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome 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.
Familial adult myoclonic epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hot water epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hot water epilepsy 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.
Familial adult myoclonic epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial adult myoclonic epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 7 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.
Idiopathic generalized epilepsy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial adult myoclonic epilepsy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial focal epilepsy with variable foci 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial focal epilepsy with variable foci 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial adult myoclonic epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial focal epilepsy with variable foci 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial focal epilepsy with variable foci 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked epilepsy with variable learning disabilities and behavior disorders Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked epilepsy with variable learning disabilities and behavior disorders in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile myoclonic epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile myoclonic epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset vitamin B6-dependent epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset vitamin B6-dependent epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Simple partial epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Simple partial epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial adult myoclonic epilepsy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adult myoclonic epilepsy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonic epilepsy of Lafora Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonic epilepsy of Lafora phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuronal ceroid lipofuscinosis 8 northern epilepsy variant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuronal ceroid lipofuscinosis 8 northern epilepsy variant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cortical dysplasia-focal epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized epilepsy 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.
Self-limited epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Self-limited epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign sporadic infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign sporadic infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe myoclonic epilepsy in infancy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe myoclonic epilepsy in infancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pyridoxine-dependent epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pyridoxine-dependent epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pyridoxine-dependent epilepsy caused by ALDH7A1 mutant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pyridoxine-dependent epilepsy caused by ALDH7A1 mutant 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.
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial focal epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial focal epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNQ1-related epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNQ1-related epilepsy 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.
Focal epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorder - epilepsy - arthrogryposis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autism spectrum disorder - epilepsy - arthrogryposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized epilepsy-paroxysmal dyskinesia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized epilepsy-paroxysmal dyskinesia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rolandic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rolandic 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.
Intellectual disability-epilepsy-extrapyramidal syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-epilepsy-extrapyramidal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epilepsy of infancy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epilepsy of infancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCN2A-related generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN2A-related generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial sleep-related hypermotor epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial sleep-related hypermotor epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PCDH19-related epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PCDH19-related epilepsy syndrome 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.
Spastic paraplegia-severe developmental delay-epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia-severe developmental delay-epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pharmacoresistant multifocal epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pharmacoresistant multifocal epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-lesional focal epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-lesional focal epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ACTL6B-related recessive epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ACTL6B-related recessive epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNAB2-related epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNAB2-related epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PCDH19-related epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PCDH19-related epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TNK2-associated Epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TNK2-associated Epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
NUS1-related epilepsy-myoclonus-ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the NUS1-related epilepsy-myoclonus-ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MICAL1-related Lateral temporal epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MICAL1-related Lateral temporal epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
BSN related epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the BSN related epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rare epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare epilepsy 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.
Epilepsy and lamotrigine-induced maculopapular eruptions Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epilepsy and lamotrigine-induced maculopapular eruptions phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to antiepileptic drugs in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antiepileptic drugs in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to valproic acid in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to lamotrigine in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to levetiracetam in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to levetiracetam in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to lamotrigine and valproic acid in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine and valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to ketogenic dietary therapies in epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ketogenic dietary therapies in epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epilepsy (remission after treatment) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epilepsy (remission after treatment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Juvenile myoclonic epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Juvenile myoclonic epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Focal epilepsy (with hippocampal sclerosis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Focal epilepsy (with hippocampal sclerosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Focal epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Focal epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

BOP Gene

ETL6 Gene

ETL2 Gene

ETL4 Gene

FMTLE Gene

KNDC1 Gene

ENFL2 Gene

Occipital Lobe Epilepsy Gene Set

epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set

Refractory Occipital Lobe Epilepsy Gene Set

Occipital Lobe Gene Set

occipital lobe Gene Set

abnormal occipital lobe morphology Gene Set

occipital lobe Gene Set

occipital lobe Gene Set

occipital lobe Gene Set

abnormal occipital lobe morphology Gene Set

Occipital lobe neoplasm Gene Set

Occipital lobe Gene Set

Occipital lobe Gene Set

Occipital lobe Gene Set

Occipital lobe volume Gene Set

Benign Occipital Epilepsy Gene Set

Childhood Benign Occipital Epilepsy Gene Set

Autosomal dominant nocturnal frontal lobe epilepsy Gene Set

Epilepsy, nocturnal frontal lobe, 5 Gene Set

Epilepsy, lateral temporal lobe, autosomal dominant Gene Set

Epilepsy, nocturnal frontal lobe, type 4 Gene Set

Epilepsy, nocturnal frontal lobe, type 3 Gene Set

Epilepsy, nocturnal frontal lobe, type 1 Gene Set

Epilepsy, Frontal Lobe Gene Set

EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set

EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set

Epilepsy, Temporal Lobe Gene Set

EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set

Epilepsy, Nocturnal Frontal Lobe, Type 4 Gene Set

Epilepsy, Nocturnal Frontal Lobe, Type 2 Gene Set

Epilepsy, Familial Temporal Lobe, 4 Gene Set

Epilepsy, Nocturnal Frontal Lobe, Type 3 Gene Set

Epilepsy, Nocturnal Frontal Lobe, Type 1 Gene Set

temporal lobe epilepsy Gene Set

epilepsy, temporal lobe; seizures, febrile Gene Set

epilepsy, temporal lobe Gene Set

epilepsy, temporal lobe; sclerosis Gene Set

epilepsy, temporal lobe; Gene Set

epilepsy, temporal lobe; sclerosis; seizures, febrile Gene Set

epilepsy, temporal lobe; memory disorders Gene Set

temporal lobe epilepsy Gene Set

confusion; epilepsy, temporal lobe; sclerosis; seizures Gene Set

nocturnal frontal lobe epilepsy Gene Set

confusion; epilepsy, temporal lobe Gene Set

epilepsy, frontal lobe Gene Set

epilepsy, frontal lobe; Gene Set

temporal lobe epilepsy Gene Set

Epilepsy, Frontal Lobe Gene Set

Epilepsy, Temporal Lobe Gene Set

epilepsy, familial temporal lobe, 5 Gene Set

epilepsy, familial temporal lobe, 4 Gene Set

epilepsy, familial temporal lobe, 6 Gene Set

epilepsy, familial temporal lobe, 1 Gene Set

epilepsy, familial temporal lobe, 2 Gene Set

epilepsy, nocturnal frontal lobe, 5 Gene Set

epilepsy, nocturnal frontal lobe, 3 Gene Set

epilepsy, nocturnal frontal lobe, 1 Gene Set

epilepsy, nocturnal frontal lobe, type 4 Gene Set

epilepsy, nocturnal frontal lobe, type 2 Gene Set

Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis Gene Set

Autosomal Dominant Lateral Temporal Lobe Epilepsy Gene Set

Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Gene Set

Benign Familial Mesial Temporal Lobe Epilepsy Gene Set

Refractory Frontal Lobe Epilepsy Gene Set

Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene Set

Familial temporal lobe epilepsy 1 Gene Set

Temporal lobe epilepsy Gene Set

Frontal lobe epilepsy Gene Set

Autosomal dominant nocturnal frontal lobe epilepsy Gene Set

Temporal lobe epilepsy Gene Set

Autosomal dominant nocturnal frontal lobe epilepsy Gene Set

Frontal lobe epilepsy Gene Set