| Name |
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Particulate Matter Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Particulate Matter from the curated CTD Gene-Chemical Interactions dataset. |
Colorectal cancer x fine particulate matter exposure levels interaction Gene SetFrom 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. |
QT interval (ambient particulate matter interaction) Gene SetFrom 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. |
White matter lesion progression (adjusted for white matter lesion burden at baseline) Gene SetFrom 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. |
particulate Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term particulate in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Cross-presentation of particulate exogenous antigens (phagosomes) Gene Setproteins participating in the Cross-presentation of particulate exogenous antigens (phagosomes) pathway from the Reactome Pathways dataset. |
Cross-presentation of particulate exogenous antigens (phagosomes) Gene Setproteins participating in the Cross-presentation of particulate exogenous antigens (phagosomes) pathway from the Reactome Pathways 2024 dataset. |
cerebellar white matter Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
verbal learning, verbal memory, and regional cortical gray matter density Gene SetFrom 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. |
intracranial hemorrhage; white matter disease Gene SetFrom 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. |
homocysteine metabolism, cognition, and white matter lesions Gene SetFrom 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 SetFrom 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. |
matter Gene SetFrom 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. |
White matter integrity Gene SetFrom 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 SetFrom 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. |
Gray matter volume (schizophrenia interaction) Gene SetFrom 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. |
White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
focal white matter lesions Gene SetFrom 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. |
periventricular gray matter heterotopia Gene SetFrom 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. |
diffuse demyelination of the cerebral white matter Gene SetFrom 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 SetFrom 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 SetFrom 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. |
gray matter heterotopias Gene SetFrom 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. |
abnormality of the brainstem white matter Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 spinal cord grey matter morphology Gene SetFrom 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. |
abnormal cerebellum white matter morphology Gene SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the leukoencephaly with vanishing white matter phenotype from the curated OMIM Gene-Disease Associations dataset. |
cerebral gray matter Gene SetFrom 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. |
cerebral white matter Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Periventricular Gray Matter Heterotopia Gene SetFrom 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. |
Diffuse Demyelination Of The Cerebral White Matter Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Focal White Matter Lesions Gene SetFrom 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. |
Hypointensity Of Cerebral White Matter On Mri Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
abnormal spinal cord grey matter morphology Gene SetFrom 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. |
Leukoencephalopathy with vanishing white matter Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Cerebral gray matter Gene SetFrom 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. |
Vanishing white matter disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vanishing white matter disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome Gene SetFrom 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. |
Abnormal cerebral white matter morphology Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Superior frontal gyrus grey matter volume Gene SetFrom 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. |
White matter microstructure (global fractional anisotropy) Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Gray matter volume (schizophrenia interaction) Gene SetFrom 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. |
Cerebellum white matter volume Gene SetFrom 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 SetFrom 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. |
Whole brain grey matter density Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Brain volume in infants (white matter) Gene SetFrom 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. |
Brain volume in infants (grey matter) Gene SetFrom 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. |