Focal white matter lesions

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Results for "Focal white matter lesions": 581 gene sets

Name
focal white matter lesions Gene Set From HPO Gene-Disease Associations genes associated with the focal white matter lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Focal White Matter Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal White Matter Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White matter lesion progression (adjusted for white matter lesion burden at baseline) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter lesion progression (adjusted for white matter lesion burden at baseline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
homocysteine metabolism, cognition, and white matter lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease homocysteine metabolism, cognition, and white matter lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral white matter lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral white matter lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Yellow/White Lesions Of The Macula Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Yellow/White Lesions Of The Macula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Yellow/White Lesions Of The Retina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Yellow/White Lesions Of The Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cerebellar white matter Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar white matter relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
white matter of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in white matter of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Leukoencephalopathy with vanishing white matter Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with vanishing white matter phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vanishing White Matter Leukodystrophy with Ovarian Failure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vanishing White Matter Leukodystrophy with Ovarian Failure from the curated CTD Gene-Disease Associations dataset.
frontal-limbic white matter pathway associations Gene Set From GAD Gene-Disease Associations genes associated with the disease frontal-limbic white matter pathway associations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral white matter hyperintensities Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral white matter hyperintensities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracranial hemorrhage; white matter disease Gene Set From GAD Gene-Disease Associations genes associated with the disease intracranial hemorrhage; white matter disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
White matter integrity Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter integrity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
White matter integrity (interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter integrity (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
White matter microstructure (global fractional anisotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter microstructure (global fractional anisotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
White matter hyperintensity burden Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter hyperintensity burden phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
abnormality of the cerebral white matter Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
hypointensity of cerebral white matter on mri Gene Set From GWASdb SNP-Phenotype Associations genes associated with the hypointensity of cerebral white matter on mri phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cerebral white matter atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
white matter neuronal heterotopia Gene Set From HPO Gene-Disease Associations genes associated with the white matter neuronal heterotopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse white matter abnormalities Gene Set From HPO Gene-Disease Associations genes associated with the diffuse white matter abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse demyelination of the cerebral white matter Gene Set From HPO Gene-Disease Associations genes associated with the diffuse demyelination of the cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse swelling of cerebral white matter Gene Set From HPO Gene-Disease Associations genes associated with the diffuse swelling of cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
deep white matter hypodensities Gene Set From HPO Gene-Disease Associations genes associated with the deep white matter hypodensities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the brainstem white matter Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the brainstem white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the periventricular white matter Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the periventricular white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multifocal cerebral white matter abnormalities Gene Set From HPO Gene-Disease Associations genes associated with the multifocal cerebral white matter abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe demyelination of the white matter Gene Set From HPO Gene-Disease Associations genes associated with the severe demyelination of the white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
patchy demyelination of subcortical white matter Gene Set From HPO Gene-Disease Associations genes associated with the patchy demyelination of subcortical white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcortical white matter calcifications Gene Set From HPO Gene-Disease Associations genes associated with the subcortical white matter calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebral white matter Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypointensity of cerebral white matter on mri Gene Set From HPO Gene-Disease Associations genes associated with the hypointensity of cerebral white matter on mri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal spinal cord white matter morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal brain white matter morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal brain white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum white matter morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
leukoencephalopathy with vanishing white matter Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with vanishing white matter phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephaly with vanishing white matter Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephaly with vanishing white matter phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral white matter Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral white matter in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Vanishing White Matter Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vanishing White Matter Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Periventricular White Matter Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Periventricular White Matter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral White Matter Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral White Matter Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse White Matter Abnormalities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse White Matter Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Demyelination Of The Cerebral White Matter Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Demyelination Of The Cerebral White Matter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periventricular White Matter Hyperdensities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periventricular White Matter Hyperdensities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multifocal Cerebral White Matter Abnormalities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multifocal Cerebral White Matter Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral White Matter Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral White Matter Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypointensity Of Cerebral White Matter On Mri Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypointensity Of Cerebral White Matter On Mri in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hyperintensity Of Cerebral White Matter On Mri Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperintensity Of Cerebral White Matter On Mri in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Patchy Demyelination Of Subcortical White Matter Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patchy Demyelination Of Subcortical White Matter in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subcortical White Matter Calcifications Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subcortical White Matter Calcifications in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Swelling Of Cerebral White Matter Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Swelling Of Cerebral White Matter in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Demyelination Of The White Matter Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Demyelination Of The White Matter in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Deep White Matter Hypodensities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deep White Matter Hypodensities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Deep Cerebral White Matter Hyperdensities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deep Cerebral White Matter Hyperdensities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal cerebellum white matter morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum white matter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal brain white matter morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain white matter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord white matter morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Leukoencephalopathy with vanishing white matter Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Leukoencephalopathy with vanishing white matter from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Leukoencephalopathy with vanishing white matter Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukoencephalopathy with vanishing white matter in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukoencephalopathy with vanishing white matter 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukoencephalopathy with vanishing white matter 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral white matter Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral white matter in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Vanishing white matter disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vanishing white matter disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal cerebral white matter morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal cerebral white matter morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
White matter deficit Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the White matter deficit phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inclusion body myopathy and brain white matter abnormalities Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy and brain white matter abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal white matter microstructure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal white matter microstructure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter hyperintensity volume x hypertension interaction (2df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensity volume x hypertension interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter hyperintensity volume (adjusted for hypertension) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensity volume (adjusted for hypertension) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter hyperintensity volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensity volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Periventricular white matter hyperintensities Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periventricular white matter hyperintensities phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Deep white matter hyperintensities Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Deep white matter hyperintensities phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter lesion progression Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter lesion progression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter hyperintensities in ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensities in ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter hyperintensity burden Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensity burden phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter microstructure in first episode schizophrenia (right posterior cingulate cortex) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure in first episode schizophrenia (right posterior cingulate cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter microstructure in first episode schizophrenia (left posterior cingulate cortex) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure in first episode schizophrenia (left posterior cingulate cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter microstructure in first episode schizophrenia (left inferior parietal cortex) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure in first episode schizophrenia (left inferior parietal cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Abnormal white matter microstructure in first episode schizophrenia (multivariate analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abnormal white matter microstructure in first episode schizophrenia (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter microstructure in first episode schizophrenia (left anterior cingulate cortex) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure in first episode schizophrenia (left anterior cingulate cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter microstructure in first episode schizophrenia (right anterior cingulate cortex) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure in first episode schizophrenia (right anterior cingulate cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter hyperintensities Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensities phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter integrity (fractional anisotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter integrity (fractional anisotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter integrity (mean diffusivity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter integrity (mean diffusivity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter growth Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter growth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Visceral fat, circulating phospholipid PC(16:0/2:0) and white matter microstructure (shared variance) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Visceral fat, circulating phospholipid PC(16:0/2:0) and white matter microstructure (shared variance) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter microstructure (global fractional anisotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure (global fractional anisotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter integrity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter integrity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter integrity (bipolar disorder risk interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter integrity (bipolar disorder risk interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebellum white matter volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebellum white matter volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebral white matter volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebral white matter volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Brain volume in infants (white matter) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brain volume in infants (white matter) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; lipoid nephrosis; nephrosis, lipoid Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; lipoid nephrosis; nephrosis, lipoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal segmental glomsclerosis; glomerulosclerosis, focal segmental; lipoid nephrosis; nephrosis, lipoid Gene Set From GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulosclerosis, focal segmental; lipoid nephrosis; nephrosis, lipoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african Gene Set From GAD Gene-Disease Associations genes associated with the disease african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal segmental glomsclerosis; glomerulosclerosis, focal segmental; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulosclerosis, focal segmental; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal segmental glomsclerosis; glomerulosclerosis, focal segmental Gene Set From GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulosclerosis, focal segmental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal segmental glomsclerosis; glomerulosclerosis, focal segmental; nephrotic syndrome; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulosclerosis, focal segmental; nephrotic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal segmental glomsclerosis; glomerulonephritis, iga; glomerulosclerosis, focal segmental; iga glomerulonephritides Gene Set From GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulonephritis, iga; glomerulosclerosis, focal segmental; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aids-associated nephropathy; focal segmental glomsclerosis; glomerulosclerosis, focal segmental Gene Set From GAD Gene-Disease Associations genes associated with the disease aids-associated nephropathy; focal segmental glomsclerosis; glomerulosclerosis, focal segmental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Atrichia with papular lesions Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrichia with papular lesions phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrichia with Papular Lesions Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrichia with Papular Lesions from the curated CTD Gene-Disease Associations dataset.
development of coronary artery lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease development of coronary artery lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain lesions or calcifications Gene Set From GAD Gene-Disease Associations genes associated with the disease brain lesions or calcifications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerotic lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerotic lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premalignant oral lesions and oral squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease premalignant oral lesions and oral squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oral premalignant lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease oral premalignant lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung cancer and preneoplastic bronchial lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease lung cancer and preneoplastic bronchial lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lesions Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term lesions in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cystic lesions of the pinnae Gene Set From HPO Gene-Disease Associations genes associated with the cystic lesions of the pinnae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
punctate vasculitis skin lesions Gene Set From HPO Gene-Disease Associations genes associated with the punctate vasculitis skin lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
profuse pigmented skin lesions Gene Set From HPO Gene-Disease Associations genes associated with the profuse pigmented skin lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
depigmented lesions of the retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the depigmented lesions of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chilblain lesions Gene Set From HPO Gene-Disease Associations genes associated with the chilblain lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized papillary lesions Gene Set From HPO Gene-Disease Associations genes associated with the generalized papillary lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral basal ganglia lesions Gene Set From HPO Gene-Disease Associations genes associated with the bilateral basal ganglia lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal cord lesions Gene Set From HPO Gene-Disease Associations genes associated with the spinal cord lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symmetric lesions of the basal ganglia Gene Set From HPO Gene-Disease Associations genes associated with the symmetric lesions of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duodenal lesions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the duodenal lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin lesions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atherosclerotic lesions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atherosclerotic lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic elastic tissue lesions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrichia with papular lesions Gene Set From OMIM Gene-Disease Associations genes associated with the atrichia with papular lesions phenotype from the curated OMIM Gene-Disease Associations dataset.
lesions Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term lesions in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Vascular Lesions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vascular Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrichia With Papular Lesions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrichia With Papular Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmented Lesions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmented Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcortical Lesions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcortical Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetric Lesions Of The Basal Ganglia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetric Lesions Of The Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lesions In The Basal Ganglia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lesions In The Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Doughnut Lesions Of Skull, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Doughnut Lesions Of Skull, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystic Lesions Of The Pinnae Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystic Lesions Of The Pinnae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Precancerous Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Precancerous Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
High-Grade Squamous Intraepithelial Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype High-Grade Squamous Intraepithelial Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitelliform-Like Macular Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitelliform-Like Macular Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bilateral Basal Ganglia Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bilateral Basal Ganglia Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Other Lesions Of Median Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Lesions Of Median Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Papillary Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Papillary Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Profuse Pigmented Skin Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Profuse Pigmented Skin Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Punctate Vasculitis Skin Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Punctate Vasculitis Skin Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
atherosclerotic lesions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atherosclerotic lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skin lesions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skin lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
duodenal lesions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the duodenal lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic elastic tissue lesions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
eye lesions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the eye lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template Gene Set From Reactome Pathways 2024 proteins participating in the Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template pathway from the Reactome Pathways 2024 dataset.
Calvarial doughnut lesions with bone fragility Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Calvarial doughnut lesions with bone fragility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrichia with papular lesions Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrichia with papular lesions in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acroosteolysis-keloid-like lesions-premature aging syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acroosteolysis-keloid-like lesions-premature aging syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KA-like vemurafenib-induced squamous lesions Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KA-like vemurafenib-induced squamous lesions phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Calvarial doughnut lesions-bone fragility syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Calvarial doughnut lesions-bone fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Calvarial doughnut lesions Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Calvarial doughnut lesions phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital left-sided heart lesions Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Congenital left-sided heart lesions phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Congenital left-sided heart lesions (maternal effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Congenital left-sided heart lesions (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary arterial lesions in patients with Kawasaki disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary arterial lesions in patients with Kawasaki disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Congenital right-sided heart lesions Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Congenital right-sided heart lesions phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Particulate Matter Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Particulate Matter from the curated CTD Gene-Chemical Interactions dataset.
verbal learning, verbal memory, and regional cortical gray matter density Gene Set From GAD Gene-Disease Associations genes associated with the disease verbal learning, verbal memory, and regional cortical gray matter density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
matter Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term matter in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Gray matter volume (schizophrenia interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Gray matter volume (schizophrenia interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
periventricular gray matter heterotopia Gene Set From HPO Gene-Disease Associations genes associated with the periventricular gray matter heterotopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gray matter heterotopias Gene Set From HPO Gene-Disease Associations genes associated with the gray matter heterotopias phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal spinal cord grey matter morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord grey matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebral gray matter Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral gray matter in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Periventricular Gray Matter Heterotopia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periventricular Gray Matter Heterotopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
abnormal spinal cord grey matter morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord grey matter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Cerebral gray matter Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral gray matter in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Superior frontal gyrus grey matter volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Superior frontal gyrus grey matter volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gray matter volume (schizophrenia interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gray matter volume (schizophrenia interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Colorectal cancer x fine particulate matter exposure levels interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colorectal cancer x fine particulate matter exposure levels interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Whole brain grey matter density Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Whole brain grey matter density phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sub-cortical grey matter volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sub-cortical grey matter volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Total grey matter volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Total grey matter volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
QT interval (ambient particulate matter interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the QT interval (ambient particulate matter interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Brain volume in infants (grey matter) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brain volume in infants (grey matter) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Focal dermal hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal dermal hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Palmoplantar keratoderma, nonepidermolytic, focal or diffuse Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Palmoplantar keratoderma, nonepidermolytic, focal or diffuse phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Palmoplantar keratoderma, nonepidermolytic, focal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Palmoplantar keratoderma, nonepidermolytic, focal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal segmental glomerulosclerosis 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal segmental glomerulosclerosis 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal segmental glomerulosclerosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal segmental glomerulosclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal segmental glomerulosclerosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal segmental glomerulosclerosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal segmental glomerulosclerosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal segmental glomerulosclerosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal segmental glomerulosclerosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal segmental glomerulosclerosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal segmental glomerulosclerosis 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal segmental glomerulosclerosis 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal segmental glomerulosclerosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal segmental glomerulosclerosis 5 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.
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.
focal adhesion Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the focal adhesion cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
focal adhesion Gene Set From COMPARTMENTS Experimental Protein Localization Evidence Scores proteins localized to the focal adhesion cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
focal adhesion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the focal adhesion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced Gene Set From CORUM Protein Complexes proteins in the Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced protein complex from the CORUM Protein Complexes dataset.
Focal Dermal Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Focal Dermal Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Focal cortical dysplasia of Taylor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Focal cortical dysplasia of Taylor from the curated CTD Gene-Disease Associations dataset.
Focal Segmental Glomerulosclerosis 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Focal Segmental Glomerulosclerosis 2 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.
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL from the curated CTD Gene-Disease Associations dataset.
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Focal Segmental Glomerulosclerosis 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Focal Segmental Glomerulosclerosis 5 from the curated CTD Gene-Disease Associations dataset.
Glomerulosclerosis, Focal Segmental Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulosclerosis, Focal Segmental from the curated CTD Gene-Disease Associations dataset.
Glomerulosclerosis, Focal Segmental Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Glomerulosclerosis, Focal Segmental in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
focal dermal hypoplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease focal dermal hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
focal epithelial hyperplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal epithelial hyperplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
focal dermal hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal dermal hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
focal segmental glomerulosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal segmental glomerulosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
focal chorioretinitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal chorioretinitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
focal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal dystonia 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.
glomerulosclerosis, focal segmental; nephrosis, lipoid Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulosclerosis, focal segmental; nephrosis, lipoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal nodular hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease focal nodular hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulosclerosis, focal segmental; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; diabetic nephropathies; glomerulosclerosis, focal segmental Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetic nephropathies; glomerulosclerosis, focal segmental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal epithelial hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease focal epithelial hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, focal Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, focal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulosclerosis, focal segmental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glomerulosclerosis, focal Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulosclerosis, focal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease focal dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term focal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
focal adhesion assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the focal adhesion assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
focal adhesion Gene Set From GO Cellular Component Annotations 2015 proteins localized to the focal adhesion cellular component from the curated GO Cellular Component Annotations 2015 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.
focal seizures Gene Set From GWASdb SNP-Phenotype Associations genes associated with the focal seizures phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal motor seizures Gene Set From GWASdb SNP-Phenotype Associations genes associated with the focal motor seizures phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal t2 hyperintense basal ganglia lesion Gene Set From HPO Gene-Disease Associations genes associated with the focal t2 hyperintense basal ganglia lesion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal seizures with impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures with impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal seizures without impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal segmental glomerulosclerosis Gene Set From HPO Gene-Disease Associations genes associated with the focal segmental glomerulosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal retinal infarction Gene Set From HPO Gene-Disease Associations genes associated with the focal retinal infarction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal seizures Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with focal epileptiform discharges Gene Set From HPO Gene-Disease Associations genes associated with the eeg with focal epileptiform discharges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal motor seizures Gene Set From HPO Gene-Disease Associations genes associated with the focal motor seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with centrotemporal focal spike waves Gene Set From HPO Gene-Disease Associations genes associated with the eeg with centrotemporal focal spike waves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with focal spike waves Gene Set From HPO Gene-Disease Associations genes associated with the eeg with focal spike waves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal dystonia Gene Set From HPO Gene-Disease Associations genes associated with the focal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the focal clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Focal Epithelial Hyperplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Focal Epithelial Hyperplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Focal Nodular Hyperplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Focal Nodular Hyperplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Glomerulosclerosis, Focal Segmental Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glomerulosclerosis, Focal Segmental phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Focal adhesion kinase, targeting (FAT) domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Focal adhesion kinase, targeting (FAT) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
focal adhesion Gene Set From KEGG Pathways proteins participating in the focal adhesion pathway from the KEGG Pathways dataset.
focal dorsal hair loss Gene Set From MPO Gene-Phenotype Associations gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
focal hair loss Gene Set From MPO Gene-Phenotype Associations gene mutations causing the focal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
focal hepatic necrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the focal hepatic necrosis phenotype in transgenic mice from the MPO 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.
focal cortical dysplasia, taylor balloon cell type Gene Set From OMIM Gene-Disease Associations genes associated with the focal cortical dysplasia, taylor balloon cell type phenotype from the curated OMIM Gene-Disease Associations dataset.
focal segmental glomerulosclerosis 8 Gene Set From OMIM Gene-Disease Associations genes associated with the focal segmental glomerulosclerosis 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
{glomerulosclerosis, focal segmental, 4, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {glomerulosclerosis, focal segmental, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
palmoplantar keratoderma, nonepidermolytic, focal or diffuse Gene Set From OMIM Gene-Disease Associations genes associated with the palmoplantar keratoderma, nonepidermolytic, focal or diffuse phenotype from the curated OMIM Gene-Disease Associations dataset.
focal dermal hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the focal dermal hypoplasia 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.
palmoplantar keratoderma, nonepidermolytic, focal Gene Set From OMIM Gene-Disease Associations genes associated with the palmoplantar keratoderma, nonepidermolytic, focal phenotype from the curated OMIM Gene-Disease Associations dataset.
focal facial dermal dysplasia 4 Gene Set From OMIM Gene-Disease Associations genes associated with the focal facial dermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the glomerulosclerosis, focal segmental, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the glomerulosclerosis, focal segmental, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the glomerulosclerosis, focal segmental, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the glomerulosclerosis, focal segmental, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the glomerulosclerosis, focal segmental, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
glomerulosclerosis, focal segmental, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the glomerulosclerosis, focal segmental, 7 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.
focal facial dermal dysplasia 3, setleis type Gene Set From OMIM Gene-Disease Associations genes associated with the focal facial dermal dysplasia 3, setleis type phenotype from the curated OMIM Gene-Disease Associations dataset.
Signaling events mediated by focal adhesion kinase Gene Set From PID Pathways proteins participating in the Signaling events mediated by focal adhesion kinase pathway from the PID Pathways dataset.
Localization of the PINCH-ILK-PARVIN complex to focal adhesions Gene Set From Reactome Pathways 2014 proteins participating in the Localization of the PINCH-ILK-PARVIN complex to focal adhesions pathway from the Reactome Pathways dataset.
Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) pathway from the Reactome Pathways dataset.
Focal Adhesion(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Focal Adhesion(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Primary Focal Segmental Glomerulosclerosis FSGS(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Primary Focal Segmental Glomerulosclerosis FSGS(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Focal Adhesion(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Focal Adhesion(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Focal Nodular Hyperplasia Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Nodular Hyperplasia Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Glomerulosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Segmental Glomerulosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Segmental Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Focal Segmental Glomerulosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Focal Segmental Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Focal Segmental Glomerulosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Focal Segmental Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Focal Segmental Glomerulosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Focal Segmental Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Nodular Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Nodular Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Cortical Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Emphysema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Emphysema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Dermal Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Dermal Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Idiopathic Focal Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Idiopathic Focal Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Telangiectatic Focal Nodular Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Telangiectatic Focal Nodular Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Focal Hyperhidrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Focal Hyperhidrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Seizures, Afebril Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Seizures, Afebril in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Epithelial Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Epithelial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cutaneous Focal Mucinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Focal Mucinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Myoclonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Myoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Thyroiditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Thyroiditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Tonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Tonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Myopathy With Focal Depletion Of Mitochondria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy With Focal Depletion Of Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Chorioretinitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Chorioretinitis 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.
Generalized Tonic-Clonic Seizures With Focal Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Tonic-Clonic Seizures With Focal Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Focal Bacterial Nephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Focal Bacterial Nephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Facial Dermal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Facial Dermal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Facial Dermal Dysplasia 4 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Facial Dermal Dysplasia 4 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Cortical Dysplasia Type Iia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia Type Iia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Palmoplantar Keratoderma With Joint Keratoses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Palmoplantar Keratoderma With Joint Keratoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Focal Dermal Elastosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Focal Dermal Elastosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Cortical Dysplasia Type Iib Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia Type Iib in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Lissencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Lissencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myositis, Focal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myositis, Focal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Sensory Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Sensory Seizure 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.
Focal Cortical Dysplasia Of Taylor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia Of Taylor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Oral Mucinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Oral Mucinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Focal Cortical Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Focal Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Seizures, Focal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Focal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal T2 Hyperintense Brainstem Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal T2 Hyperintense Brainstem Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal Neurologic Deficits Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal Neurologic Deficits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Temporal Focal Spikes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Temporal Focal Spikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal T2 Hyperintense Basal Ganglia Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal T2 Hyperintense Basal Ganglia Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal T2 Hypointense Brainstem Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal T2 Hypointense Brainstem Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal Segmental Glomerulosclerosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal Segmental Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Focal Sharp Slow Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Sharp Slow Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Focal Spikes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Spikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal T2 Hypointense Basal Ganglia Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal T2 Hypointense Basal Ganglia Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Central Focal Spikes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Central Focal Spikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Focal Spike Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Spike Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Centrotemporal Focal Spike Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Centrotemporal Focal Spike Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Focal Sharp Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Sharp Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal Eeg Discharges With Secondary Generalization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal Eeg Discharges With Secondary Generalization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal Sensory Auditory Seizure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal Sensory Auditory Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Parietal Focal Spikes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Parietal Focal Spikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal T2 Hyperintense Thalamic Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal T2 Hyperintense Thalamic Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal T2 Hypointense Thalamic Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal T2 Hypointense Thalamic Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Focal Epileptiform Discharges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Epileptiform Discharges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
focal adhesion assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the focal adhesion assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of focal adhesion disassembly Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of focal adhesion disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of focal adhesion disassembly Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of focal adhesion disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.
focal adhesion Gene Set From GO Cellular Component Annotations 2023 proteins localized to the focal adhesion cellular component from the curated GO Cellular Component Annotations 2023 dataset.
focal hepatic necrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hepatic necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
focal hair loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
focal hair loss in head/neck region Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in head/neck region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
focal dorsal hair loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
focal hair loss in abdominal region Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in abdominal region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
focal hair loss in thorax region Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in thorax region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Primary focal segmental glomerulosclerosis FSGS Gene Set From WikiPathways Pathways 2024 proteins participating in the Primary focal segmental glomerulosclerosis FSGS pathway from the WikiPathways Pathways 2024 dataset.
Focal adhesion Gene Set From WikiPathways Pathways 2024 proteins participating in the Focal adhesion pathway from the WikiPathways Pathways 2024 dataset.
Focal adhesion PI3K Akt mTOR signaling Gene Set From WikiPathways Pathways 2024 proteins participating in the Focal adhesion PI3K Akt mTOR signaling pathway from the WikiPathways Pathways 2024 dataset.
Localization of the PINCH-ILK-PARVIN complex to focal adhesions Gene Set From Reactome Pathways 2024 proteins participating in the Localization of the PINCH-ILK-PARVIN complex to focal adhesions pathway from the Reactome Pathways 2024 dataset.
focal adhesion assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the focal adhesion assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of focal adhesion assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of focal adhesion assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of focal adhesion disassembly Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of focal adhesion disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of focal adhesion disassembly Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of focal adhesion disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.
focal adhesion Gene Set From GO Cellular Component Annotations 2025 proteins localized to the focal adhesion cellular component from the curated GO Cellular Component Annotations 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.
Focal dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Focal dystonia 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.
Focal dermal hypoplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Focal dermal hypoplasia from the DISEASES Curated Gene-Disease Association 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.
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.
Focal segmental glomerulosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal hand dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal hand dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal dermal hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal dermal hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal chorioretinitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal chorioretinitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal epithelial hyperplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal epithelial hyperplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal nonepidermolytic palmoplantar keratoderma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal nonepidermolytic palmoplantar keratoderma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal segmental glomerulosclerosis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 1 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.
Focal or diffuse nonepidermolytic palmoplantar keratoderma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal or diffuse nonepidermolytic palmoplantar keratoderma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal segmental glomerulosclerosis 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Unilateral focal polymicrogyria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Unilateral focal polymicrogyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal segmental glomerulosclerosis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 2 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.
Focal segmental glomerulosclerosis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal segmental glomerulosclerosis 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 7 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.
Focal segmental glomerulosclerosis 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal segmental glomerulosclerosis 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal segmental glomerulosclerosis 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal segmental glomerulosclerosis 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal adhesion Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Focal adhesion cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Focal adhesion Gene Set From COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 proteins localized to the Focal adhesion cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
Focal adhesion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Focal adhesion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Focal segmental glomerulosclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal segmental glomerulosclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated focal cortical dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated focal cortical dysplasia 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.
Focal-onset seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal-onset seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Focal dermal hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal dermal hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Focal T2 hyperintense basal ganglia lesion Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal T2 hyperintense basal ganglia lesion 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.
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.
Early onset focal segmental glomerulosclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset focal segmental glomerulosclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated focal non-epidermolytic palmoplantar keratoderma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated focal non-epidermolytic palmoplantar keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Focal impaired awareness seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal impaired awareness seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Focal cortical dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal cortical dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inherited focal segmental glomerulosclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited focal segmental glomerulosclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Focal segmental glomerulosclerosis and neurodevelopmental syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal segmental glomerulosclerosis and neurodevelopmental syndrome 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.
Focal and segmental glomerulosclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal and segmental glomerulosclerosis phenotype from the curated ClinVar Gene-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.
Focal adhesion Gene Set From KEGG Pathways 2026 proteins participating in the Focal adhesion pathway from the KEGG Pathways 2026 dataset.
Superior colliculus, motor related, intermediate white layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
intermediate white layer of SC Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in intermediate white layer of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, deep white layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, deep white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
deep white layer of SC Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in deep white layer of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
White sponge nevus of cannon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the White sponge nevus of cannon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wolff-Parkinson-White Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wolff-Parkinson-White Syndrome from the curated CTD Gene-Disease Associations dataset.
wolff-parkinson-white syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease wolff-parkinson-white syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
white piedra Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease white piedra in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
wolff-parkinson-white syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease wolff-parkinson-white syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
white Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term white in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
CIDEC_KO_GDS3776_552_mouse_Brown and white adipose tissues Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the CIDEC_KO_GDS3776_552_mouse_Brown and white adipose tissues gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PRDM16_DEPLETION_GDS4021_460_mouse_WAT - white adipose tissue (stromal-vascular cells) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PRDM16_DEPLETION_GDS4021_460_mouse_WAT - white adipose tissue (stromal-vascular cells) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
SFRP5_KO_GDS4988_27_mouse_gonadal white adipose tissue HFD Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SFRP5_KO_GDS4988_27_mouse_gonadal white adipose tissue HFD gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
white fat cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the white fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of white fat cell proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of white fat cell proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
White blood cell count Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
White blood cell types Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White blood cell types phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
C-reactive protein and white blood cell count Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the C-reactive protein and white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
white forelock Gene Set From HPO Gene-Disease Associations genes associated with the white forelock phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
white eyelashes Gene Set From HPO Gene-Disease Associations genes associated with the white eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
white eyebrow Gene Set From HPO Gene-Disease Associations genes associated with the white eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
wolff-parkinson-white syndrome Gene Set From HPO Gene-Disease Associations genes associated with the wolff-parkinson-white syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
white hair Gene Set From HPO Gene-Disease Associations genes associated with the white hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
white mater abnormalities in the posterior periventricular region Gene Set From HPO Gene-Disease Associations genes associated with the white mater abnormalities in the posterior periventricular region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Wolff-Parkinson-White Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Wolff-Parkinson-White Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Suppressor of white apricot N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Suppressor of white apricot N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
increased white fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased white adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
white spotting Gene Set From MPO Gene-Phenotype Associations gene mutations causing the white spotting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spleen white pulp amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spleen white pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white fat cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spleen white pulp morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen white pulp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased white fat cell size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intermingled spleen red and white pulp Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intermingled spleen red and white pulp phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased spleen white pulp amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased spleen white pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased white fat cell lipid droplet size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white adipose tissue physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent spleen white pulp Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent spleen white pulp phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white fat cell lipid droplet size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white adipose tissue morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white adipose tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white fat cell size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased white fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white fat cell differentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell differentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased white fat cell lipid droplet size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased white adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased white fat cell size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
[white blood cell count qtl] Gene Set From OMIM Gene-Disease Associations genes associated with the [white blood cell count qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.
wolff-parkinson-white syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the wolff-parkinson-white syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
white sponge nevus 1 Gene Set From OMIM Gene-Disease Associations genes associated with the white sponge nevus 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
white sponge nevus 2 Gene Set From OMIM Gene-Disease Associations genes associated with the white sponge nevus 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Transcriptional regulation of white adipocyte differentiation Gene Set From Reactome Pathways 2014 proteins participating in the Transcriptional regulation of white adipocyte differentiation pathway from the Reactome Pathways dataset.
white adipose tissue Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue white adipose tissue from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
white adipose tissue Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue white adipose tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
egg white Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue egg white in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
white prepupa Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue white prepupa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Wolff-Parkinson-White Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wolff-Parkinson-White Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
May-White Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease May-White Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
White Coat Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease White Coat Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dental White Spot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dental White Spot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Evanescent White Dot Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Evanescent White Dot Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
White Sponge Nevus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease White Sponge Nevus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
White Sutton Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease White Sutton Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
White Blood Cell Count Procedure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Blood Cell Count Procedure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Blood Cell Abnormality Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Blood Cell Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Blood Cell Count Quantitative Trait Locus 1 Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Blood Cell Count Quantitative Trait Locus 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Scaling Skin Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Scaling Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Wolff-Parkinson-White Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wolff-Parkinson-White Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Hair Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Eyebrow Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Eyelashes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Forelock Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Forelock in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bland White Garland Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bland White Garland Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
White Mater Abnormalities In The Posterior Periventricular Region Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Mater Abnormalities In The Posterior Periventricular Region in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
white fat cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the white fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
white fat cell proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the white fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of white fat cell proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of white fat cell proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal spleen white pulp morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spleen white pulp morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
white spotting Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the white spotting phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased white adipose tissue amount Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white adipose tissue amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased spleen white pulp amount Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spleen white pulp amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased white adipose tissue amount Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white adipose tissue amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased white fat cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased spleen white pulp amount Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spleen white pulp amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal white adipose tissue morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white adipose tissue morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal white fat cell size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent spleen white pulp Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent spleen white pulp phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal white adipose tissue physiology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased white fat cell lipid droplet size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased white adipose tissue mass Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white adipose tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased white fat cell size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal white fat cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white fat cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intermingled spleen red and white pulp Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intermingled spleen red and white pulp phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased white fat cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased white fat cell size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased white fat cell lipid droplet size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal white fat cell differentation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white fat cell differentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal white adipose tissue amount Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white adipose tissue amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased white adipose tissue mass Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white adipose tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
browned white adipose tissue morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the browned white adipose tissue morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
white pupil Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the white pupil phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
t70-white-adipose_male_2w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_male_2w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_female_8w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_female_8w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_male_1w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_male_1w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_female_2w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_female_2w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_male_8w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_male_8w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_male_4w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_male_4w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_female_4w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_female_4w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_female_1w Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_female_1w relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
t70-white-adipose_consensus Gene Set From MoTrPAC Rat Endurance Exercise Training genes with high or low expression in t70-white-adipose_consensus relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
White fat cell_Adipose tissue_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White fat cell_Adipose tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
White preadipocyte_Adipose tissue_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White preadipocyte_Adipose tissue_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Epithelium_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Embryo_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Skeletal muscle_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Skeletal muscle_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Lymphoid tissue_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Lymphoid tissue_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Bronchus_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Bronchus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Nasal polyp_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Nasal polyp_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
White blood cell_Pancreas_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the White blood cell_Pancreas_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Differentiation of white and brown adipocyte Gene Set From WikiPathways Pathways 2024 proteins participating in the Differentiation of white and brown adipocyte pathway from the WikiPathways Pathways 2024 dataset.
White fat cell differentiation Gene Set From WikiPathways Pathways 2024 proteins participating in the White fat cell differentiation pathway from the WikiPathways Pathways 2024 dataset.
Transcriptional regulation of white adipocyte differentiation Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional regulation of white adipocyte differentiation pathway from the Reactome Pathways 2024 dataset.
white fat cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the white fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
white fat cell proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the white fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of white fat cell proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of white fat cell proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
White sponge nevus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease White sponge nevus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
White-Sutton syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease White-Sutton syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Wolff-Parkinson-White syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Wolff-Parkinson-White syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Wolff-Parkinson-White syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Wolff-Parkinson-White syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
White piedra Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease White piedra in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
White sponge nevus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease White sponge nevus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
White-Sutton syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease White-Sutton syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
White sponge nevus 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease White sponge nevus 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
White adipose tissue Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue White adipose tissue from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
White adipose tissue Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue White adipose tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Egg white Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Egg white in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Epididymal white adipose tissue Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Epididymal white adipose tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
White prepupa Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue White prepupa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Wolff-Parkinson-White pattern Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Wolff-Parkinson-White pattern phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
White sponge nevus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the White sponge nevus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lymphocyte percentage of white cells Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lymphocyte percentage of white cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White blood cell count Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neutrophil percentage of white cells Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neutrophil percentage of white cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Monocyte percentage of white cells Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Monocyte percentage of white cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Granulocyte percentage of myeloid white cells Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Granulocyte percentage of myeloid white cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Eosinophil percentage of white cells Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eosinophil percentage of white cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White blood cell count (basophil) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White blood cell count (basophil) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Myeloid white cell count Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Myeloid white cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Basophil percentage of white cells Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Basophil percentage of white cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mitochondrial DNA copy number (white blood cells) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mitochondrial DNA copy number (white blood cells) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White wine liking Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White wine liking phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White blood cell types Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White blood cell types phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
C-reactive protein and white blood cell count Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the C-reactive protein and white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Low white blood cell count Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Low white blood cell count (conditioned on rs2814778) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low white blood cell count (conditioned on rs2814778) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White blood cell count (eosinophil) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White blood cell count (eosinophil) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White blood cell count (lymphocyte) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White blood cell count (lymphocyte) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White blood cell count (monocyte) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White blood cell count (monocyte) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White blood cell count (neutrophil) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White blood cell count (neutrophil) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White coat effect (clinic systolic blood pressure minus ambulatory systolic blood pressure) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White coat effect (clinic systolic blood pressure minus ambulatory systolic blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White coat effect (clinic diastolic blood pressure minus ambulatory diastolic blood pressure) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White coat effect (clinic diastolic blood pressure minus ambulatory diastolic blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

focal white matter lesions Gene Set

Focal White Matter Lesions Gene Set

White matter lesion progression (adjusted for white matter lesion burden at baseline) Gene Set

homocysteine metabolism, cognition, and white matter lesions Gene Set

cerebral white matter lesions Gene Set

Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome Gene Set

Yellow/White Lesions Of The Macula Gene Set

Yellow/White Lesions Of The Retina Gene Set

cerebellar white matter Gene Set

white matter of cerebellar vermis Gene Set

Leukoencephalopathy with vanishing white matter Gene Set

Vanishing White Matter Leukodystrophy with Ovarian Failure Gene Set

frontal-limbic white matter pathway associations Gene Set

cerebral white matter hyperintensities Gene Set

intracranial hemorrhage; white matter disease Gene Set

White matter integrity Gene Set

White matter integrity (interaction) Gene Set

White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

White matter microstructure (global fractional anisotropy) Gene Set

White matter hyperintensity burden Gene Set

abnormality of the cerebral white matter Gene Set

hypointensity of cerebral white matter on mri Gene Set

cerebral white matter atrophy Gene Set

white matter neuronal heterotopia Gene Set

diffuse white matter abnormalities Gene Set

diffuse demyelination of the cerebral white matter Gene Set

diffuse swelling of cerebral white matter Gene Set

deep white matter hypodensities Gene Set

abnormality of the brainstem white matter Gene Set

abnormality of the periventricular white matter Gene Set

multifocal cerebral white matter abnormalities Gene Set

severe demyelination of the white matter Gene Set

patchy demyelination of subcortical white matter Gene Set

subcortical white matter calcifications Gene Set

abnormality of the cerebral white matter Gene Set

hypointensity of cerebral white matter on mri Gene Set

abnormal spinal cord white matter morphology Gene Set

abnormal brain white matter morphology Gene Set

abnormal cerebellum white matter morphology Gene Set

leukoencephalopathy with vanishing white matter Gene Set

leukoencephaly with vanishing white matter Gene Set

cerebral white matter Gene Set

Vanishing White Matter Disease Gene Set

Abnormality Of The Periventricular White Matter Gene Set

Cerebral White Matter Atrophy Gene Set

Diffuse White Matter Abnormalities Gene Set

Diffuse Demyelination Of The Cerebral White Matter Gene Set

Periventricular White Matter Hyperdensities Gene Set

Multifocal Cerebral White Matter Abnormalities Gene Set

Cerebral White Matter Hypoplasia Gene Set

Hypointensity Of Cerebral White Matter On Mri Gene Set

Hyperintensity Of Cerebral White Matter On Mri Gene Set

Patchy Demyelination Of Subcortical White Matter Gene Set

Subcortical White Matter Calcifications Gene Set

Diffuse Swelling Of Cerebral White Matter Gene Set

Severe Demyelination Of The White Matter Gene Set

Deep White Matter Hypodensities Gene Set

Deep Cerebral White Matter Hyperdensities Gene Set

abnormal cerebellum white matter morphology Gene Set

abnormal brain white matter morphology Gene Set

abnormal spinal cord white matter morphology Gene Set

Leukoencephalopathy with vanishing white matter Gene Set

Leukoencephalopathy with vanishing white matter Gene Set

Leukoencephalopathy with vanishing white matter 5 Gene Set

Cerebral white matter Gene Set

Vanishing white matter disease Gene Set

Abnormal cerebral white matter morphology Gene Set

White matter deficit Gene Set

Inclusion body myopathy and brain white matter abnormalities Gene Set

Neonatal white matter microstructure Gene Set

White matter hyperintensity volume x hypertension interaction (2df) Gene Set

White matter hyperintensity volume (adjusted for hypertension) Gene Set

White matter hyperintensity volume Gene Set

Periventricular white matter hyperintensities Gene Set

Deep white matter hyperintensities Gene Set

White matter lesion progression Gene Set

White matter hyperintensities in ischemic stroke Gene Set

White matter hyperintensity burden Gene Set

White matter microstructure in first episode schizophrenia (right posterior cingulate cortex) Gene Set