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Results for "brain edema; cerebral hemorrhage;": 1001 gene sets

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brain edema; cerebral hemorrhage; Gene Set From GAD Gene-Disease Associations genes associated with the disease brain edema; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain edema; brain hemorrhage, traumatic Gene Set From GAD Gene-Disease Associations genes associated with the disease brain edema; brain hemorrhage, traumatic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; cerebral infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral amyloid angiopathy; cerebral hemorrhage; cerebral hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain edema; infarction, middle cerebral artery Gene Set From GAD Gene-Disease Associations genes associated with the disease brain edema; infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cerebral hemorrhage; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain infarction; cadasil; cerebral hemorrhage; Gene Set From GAD Gene-Disease Associations genes associated with the disease brain infarction; cadasil; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain edema; brain injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease brain edema; brain injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal diseases; gastrointestinal hemorrhage; peptic ulcer; peptic ulcer hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal diseases; gastrointestinal hemorrhage; peptic ulcer; peptic ulcer hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral edema Gene Set From HPO Gene-Disease Associations genes associated with the cerebral edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebral edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
High Altitude Cerebral Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High Altitude Cerebral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fulminant Hepatic Failure With Cerebral Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fulminant Hepatic Failure With Cerebral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cytotoxic Cerebral Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cytotoxic Cerebral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vasogenic Cerebral Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vasogenic Cerebral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cerebral edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
brain concussion; brain injuries; brain ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease brain concussion; brain injuries; brain ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral hemorrhage with amyloidosis, hereditary, Dutch type from the curated CTD Gene-Disease Associations dataset.
Cerebral Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Hemorrhage from the curated CTD Gene-Disease Associations dataset.
cerebral amyloid angiopathy-related hemorrhage. Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy-related hemorrhage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; memory disorders; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; memory disorders; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; intracranial arteriovenous malformations Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; intracranial arteriovenous malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; leukomalacia, periventricular; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; leukomalacia, periventricular; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent cerebral hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the recurrent cerebral hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the cerebral hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cerebral Hemorrhage, Traumatic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebral Hemorrhage, Traumatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebral Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebral Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Cerebral Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal akinesia-cerebral and retinal hemorrhage syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal akinesia-cerebral and retinal hemorrhage syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Brain Edema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brain Edema from the curated CTD Gene-Disease Associations dataset.
brain edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
Brain Edema Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Brain Edema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Brain Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brain Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cytotoxic Brain Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cytotoxic Brain Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vasogenic Brain Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vasogenic Brain Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Brain edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brain edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Brain small vessel disease with hemorrhage Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brain Small Vessel Disease with Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.
brain hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain hemorrhage; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain hemorrhage; cerebrovascular disease; thrombosis, deep vein Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; cerebrovascular disease; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; subarachnoid hemorrhage; vasospasm, intracranial Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; subarachnoid hemorrhage; vasospasm, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain hemorrhage; stroke; stroke, lacunar Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; stroke; stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Brain Hemorrhage, Traumatic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Brain Hemorrhage, Traumatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
{intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Brain Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brain Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarct; cerebral arteriopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarct; cerebral arteriopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain infarction; cerebral arterial diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease brain infarction; cerebral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cerebral arterial diseases; intracranial embolism; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral arterial diseases; intracranial embolism; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cerebral infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism Gene Set From GAD Gene-Disease Associations genes associated with the disease brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; infarction, middle cerebral artery; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; hypoxia-ischemia, brain Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; hypoxia-ischemia, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain infarction; brain ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease brain infarction; brain ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain damage, chronic; brain injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease brain damage, chronic; brain injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain concussion; brain injuries; unconsciousness Gene Set From GAD Gene-Disease Associations genes associated with the disease brain concussion; brain injuries; unconsciousness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asphyxia neonatorum; brain ischemia; hypoxia-ischemia, brain Gene Set From GAD Gene-Disease Associations genes associated with the disease asphyxia neonatorum; brain ischemia; hypoxia-ischemia, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain damage, chronic; hypoxia-ischemia, brain; infant, newborn, diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease brain damage, chronic; hypoxia-ischemia, brain; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain hypoxia; burns; hypoxia, brain; spinal cord injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hypoxia; burns; hypoxia, brain; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Brain volume in infants (intracranial brain volume) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brain volume in infants (intracranial brain volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Edema, Cardiac Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Edema, Cardiac from the curated CTD Gene-Disease Associations dataset.
Edema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Edema from the curated CTD Gene-Disease Associations dataset.
Pulmonary Edema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Edema from the curated CTD Gene-Disease Associations dataset.
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema from the curated CTD Gene-Disease Associations dataset.
Macular Edema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Edema from the curated CTD Gene-Disease Associations dataset.
pulmonary edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cystoid macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cystoid macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetic macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diabetic macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
edema; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; edema Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema rosiglitazone or pioglitazone Gene Set From GAD Gene-Disease Associations genes associated with the disease edema rosiglitazone or pioglitazone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
altitude sickness; chromosome deletion; pulmonary edema Gene Set From GAD Gene-Disease Associations genes associated with the disease altitude sickness; chromosome deletion; pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular edema Gene Set From GAD Gene-Disease Associations genes associated with the disease macular edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary edema Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema; hypertension; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; hypertension; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinopathy, diabetic; macular edema Gene Set From GAD Gene-Disease Associations genes associated with the disease retinopathy, diabetic; macular edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema; inflammation; pre-eclampsia; proteinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; inflammation; pre-eclampsia; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
altitude sickness; pulmonary edema Gene Set From GAD Gene-Disease Associations genes associated with the disease altitude sickness; pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
type 2 diabetes; edema ; rosiglitazone Gene Set From GAD Gene-Disease Associations genes associated with the disease type 2 diabetes; edema ; rosiglitazone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
high-altitude pulmonary edema. Gene Set From GAD Gene-Disease Associations genes associated with the disease high-altitude pulmonary edema. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema; malnutrition Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema; protein-energy malnutrition Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; protein-energy malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term edema in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
edema Gene Set From GWASdb SNP-Phenotype Associations genes associated with the edema phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
hypoproteinemic edema Gene Set From HPO Gene-Disease Associations genes associated with the hypoproteinemic edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pharyngeal edema Gene Set From HPO Gene-Disease Associations genes associated with the pharyngeal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
edema of the dorsum of hands Gene Set From HPO Gene-Disease Associations genes associated with the edema of the dorsum of hands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
palpebral edema Gene Set From HPO Gene-Disease Associations genes associated with the palpebral edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intestinal edema Gene Set From HPO Gene-Disease Associations genes associated with the intestinal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular edema Gene Set From HPO Gene-Disease Associations genes associated with the muscular edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
edema of the dorsum of feet Gene Set From HPO Gene-Disease Associations genes associated with the edema of the dorsum of feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
periorbital edema Gene Set From HPO Gene-Disease Associations genes associated with the periorbital edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
edema Gene Set From HPO Gene-Disease Associations genes associated with the edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
laryngeal edema Gene Set From HPO Gene-Disease Associations genes associated with the laryngeal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular edema Gene Set From HPO Gene-Disease Associations genes associated with the macular edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized edema Gene Set From HPO Gene-Disease Associations genes associated with the generalized edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystoid macular edema Gene Set From HPO Gene-Disease Associations genes associated with the cystoid macular edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
edema of the lower limbs Gene Set From HPO Gene-Disease Associations genes associated with the edema of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
facial edema Gene Set From HPO Gene-Disease Associations genes associated with the facial edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corneal stromal edema Gene Set From HPO Gene-Disease Associations genes associated with the corneal stromal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Angioneurotic Edema Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Angioneurotic Edema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Edema Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Edema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pulmonary Edema Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Edema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Macular Edema Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Macular Edema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Macular Edema, Cystoid Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Macular Edema, Cystoid phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
intestinal edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intestinal edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
periorbital edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the periorbital edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
extremity edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the extremity edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
nuchal edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the nuchal edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary alveolar edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cardiac edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cardiac edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pericardial edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pericardial edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
eyelid edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the eyelid edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema Gene Set From OMIM Gene-Disease Associations genes associated with the dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema phenotype from the curated OMIM Gene-Disease Associations dataset.
Acute Cardiac Pulmonary Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cardiac Pulmonary Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
High Altitude Pulmonary Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High Altitude Pulmonary Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Edema, Cystoid Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Edema, Cystoid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facial Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facial Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Retinal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Retinal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exudative Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exudative Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudophakic Corneal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudophakic Corneal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fine Corneal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fine Corneal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Edema Of Legs Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Edema Of Legs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurogenic Pulmonary Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurogenic Pulmonary Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Clinically Significant Macular Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Clinically Significant Macular Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, And Perinatal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, And Perinatal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pulmonary Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pulmonary Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Edema Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Edema Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Periorbital Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periorbital Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Periorbital Edema, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periorbital Edema, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Edema, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Edema, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Corneal Stromal Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Stromal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pitting Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pitting Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intestinal Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intestinal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ankle Edema (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ankle Edema (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Transient Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acute Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thalamic Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thalamic Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Genital Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genital Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Genital Edema, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genital Edema, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Laryngeal Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Laryngeal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limbal Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limbal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Massive Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Massive Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypoproteinemic Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypoproteinemic Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skin edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skin edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pericardial edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pericardial edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
periorbital edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the periorbital edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pulmonary edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intestinal edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intestinal edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
extremity edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the extremity edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cardiac edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
eyelid edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the eyelid edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pulmonary alveolar edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary alveolar edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
generalized edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the generalized edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subcutaneous edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subcutaneous edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nuchal edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nuchal edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retropharyngeal edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retropharyngeal edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retropleural edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retropleural edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
edema Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the edema phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulmonary edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cystoid macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cystoid macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary angioneurotic edema Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary angioneurotic edema phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pedal edema Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pedal edema phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diabetic macular edema in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic macular edema in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Peptic Ulcer Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peptic Ulcer Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Uterine Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Uterine Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Postoperative Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Subarachnoid Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Subarachnoid Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Gastrointestinal Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gastrointestinal Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Retinal Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Intracranial Hemorrhage, Traumatic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Hemorrhage, Traumatic from the curated CTD Gene-Disease Associations dataset.
hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hemorrhage; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hemorrhage; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; hypertension; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysmal subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysmal subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vascular disease; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease vascular disease; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
peptic ulcer; peptic ulcer hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease peptic ulcer; peptic ulcer hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; thromboembolism; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; thromboembolism; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; hemorrhagic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; hemorrhagic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; thrombosis; von willebrand disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; thrombosis; von willebrand disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal hemorrhage; henoch-schoenlein purpura; kidney diseases; purpura, schoenlein-henoch; vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; henoch-schoenlein purpura; kidney diseases; purpura, schoenlein-henoch; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart diseases; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease heart diseases; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracranial aneurysm; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, ruptured; aortic aneurysm, abdominal; intracranial aneurysm; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; coronary thrombosis; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary thrombosis; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
postoperative complications; postoperative hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease postoperative complications; postoperative hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subconjunctival hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease subconjunctival hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal hemorrhage; helicobacter infections; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriovenous malformations; congenital arteriovenous malformation; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subarachnoid hemorrhage; vasospasm, intracranial Gene Set From GAD Gene-Disease Associations genes associated with the disease subarachnoid hemorrhage; vasospasm, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
esophageal and gastric varices; gastrointestinal hemorrhage; liver cirrhosis; postoperative complications; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease esophageal and gastric varices; gastrointestinal hemorrhage; liver cirrhosis; postoperative complications; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, ruptured; intracranial aneurysm; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; intracranial aneurysm; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; atrial fibrillation; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; atrial fibrillation; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal hemorrhage; Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; placenta diseases; premature birth; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; placenta diseases; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gingival hemorrhage; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease gingival hemorrhage; periodontal pocket; periodontitis 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.
choroid diseases; peripheral vascular diseases; vitreous hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; peripheral vascular diseases; vitreous hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hemophilia b; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hemophilia b; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
factor vii deficiency; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease factor vii deficiency; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
peptic ulcer hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease peptic ulcer hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; recurrence; thromboembolism; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; recurrence; thromboembolism; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; von willebrand diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; von willebrand diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, ruptured; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal hemorrhage; hemorrhoids; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; hemorrhoids; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracerebral hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease intracerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
postoperative hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease postoperative hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; hemorrhage; recurrence; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; hemorrhage; recurrence; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, ruptured; intracranial aneurysm; recurrence; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; intracranial aneurysm; recurrence; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; intracranial aneurysm Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; intracranial aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage, intracerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage, intracerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysmal subarachnoid hemorrhage. Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysmal subarachnoid hemorrhage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
craniocerebral trauma; hypotension; injuries, craniocerebral; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease craniocerebral trauma; hypotension; injuries, craniocerebral; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hemorrhage in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
internal hemorrhage Gene Set From GWASdb SNP-Phenotype Associations genes associated with the internal hemorrhage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
gastrointestinal hemorrhage Gene Set From GWASdb SNP-Phenotype Associations genes associated with the gastrointestinal hemorrhage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
subarachnoid hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the subarachnoid hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gastrointestinal hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the gastrointestinal hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the joint hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
internal hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the internal hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hemorrhage of the eye Gene Set From HPO Gene-Disease Associations genes associated with the hemorrhage of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the retinal hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vitreous hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the vitreous hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcutaneous hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the subcutaneous hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
antenatal intracerebral hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the antenatal intracerebral hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intracranial hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the intracranial hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Eye Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Peptic Ulcer Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Peptic Ulcer Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Postoperative Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Postoperative Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Subarachnoid Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Subarachnoid Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Intracranial Hemorrhage, Hypertensive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Intracranial Hemorrhage, Hypertensive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Gingival Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Gingival Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Gastrointestinal Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Gastrointestinal Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Postpartum Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Postpartum Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Basal Ganglia Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Basal Ganglia Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
genital hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the genital hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
brainstem hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the brainstem hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
uterine hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the uterine hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
gastrointestinal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the gastrointestinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
eye hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the eye hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
remittent intestinal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the remittent intestinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
glomerulus hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the glomerulus hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
umbilical cord hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the umbilical cord hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
internal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the internal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lung hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lung hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intraventricular hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intraventricular hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ovary hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
rectal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the rectal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intracerebral hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intracerebral hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary alveolar hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intracranial hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intracranial hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
liver hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the liver hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{hemorrhage, intracerebral, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hemorrhage, intracerebral, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Subarachnoid Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subarachnoid Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcutaneous Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcutaneous Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nontraumatic Subarachnoid Hemorrhage, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nontraumatic Subarachnoid Hemorrhage, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Alveolar Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Alveolar Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemorrhage, Intracerebral, Susceptibility To Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemorrhage, Intracerebral, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Gastrointestinal Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Gastrointestinal Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Alveolar Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Alveolar Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gastrointestinal Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gastrointestinal Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gingival Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gingival Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Perinatal Subarachnoid Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Perinatal Subarachnoid Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subarachnoid Hemorrhage, Aneurysmal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subarachnoid Hemorrhage, Aneurysmal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subarachnoid Hemorrhage, Intracranial Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subarachnoid Hemorrhage, Intracranial in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subarachnoid Hemorrhage, Spontaneous Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subarachnoid Hemorrhage, Spontaneous in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peptic Ulcer Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peptic Ulcer Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intestinal Hemorrhage Nos Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intestinal Hemorrhage Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subretinal Pigment Epithelium Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subretinal Pigment Epithelium Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventricular Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitreous Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitreous Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Internal Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Internal Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Perinatal Pulmonary Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Perinatal Pulmonary Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pulmonary Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pulmonary Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Antenatal Intracerebral Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Antenatal Intracerebral Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Intrapulmonary Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Intrapulmonary Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Antepartum Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Antepartum Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Antepartum Hemorrhage Affecting Fetus Or Newborn Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Antepartum Hemorrhage Affecting Fetus Or Newborn in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Postpartum Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postpartum Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spontaneous Intracranial Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous Intracranial Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Fossa Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Fossa Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Uterine Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uterine Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Choroid Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choroid Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Oral Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oral Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intracerebral hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intracerebral hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
internal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the internal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intracranial hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intracranial hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spinal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
placenta hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the placenta hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
remittent intestinal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the remittent intestinal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
gastrointestinal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the gastrointestinal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intraventricular hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intraventricular hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lung hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lung hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pulmonary alveolar hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary alveolar hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
liver hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the liver hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
rectal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the rectal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intestinal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intestinal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ovary hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
uterine hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the uterine hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skin hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skin hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
heart hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the heart hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lymph node hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lymph node hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subarachnoid hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subarachnoid hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subcutaneous hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subcutaneous hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small intestine hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small intestine hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
glomerulus hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the glomerulus hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
umbilical cord hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the umbilical cord hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vaginal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vaginal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
stomach hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the stomach hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
eye hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the eye hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
testicular hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the testicular hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
brainstem hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the brainstem hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subdural hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subdural hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
muscle hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscle hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hemorrhage Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the hemorrhage phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
eye hemorrhage Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the eye hemorrhage phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Hemorrhage Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intraventricular hemorrhage Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intraventricular hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intracranial hemorrhage Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intracranial hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intracerebral hemorrhage Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intracerebral hemorrhage phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-lobar intracerebral hemorrhage Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-lobar intracerebral hemorrhage phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lobar intracerebral hemorrhage Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lobar intracerebral hemorrhage phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-lobar intracerebral hemorrhage (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-lobar intracerebral hemorrhage (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebral nuclei Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cerebral nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cerebral cortex Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cerebral cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Frontal pole, cerebral cortex Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Frontal pole, cerebral cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral folate deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral folate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral palsy, spastic quadriplegic, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral palsy, spastic quadriplegic, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination, global cerebral Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination, global cerebral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral cavernous malformations 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral cavernous malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral cavernous malformations 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral cavernous malformations 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cerebral amyloid angiopathy, Icelandic type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cerebral amyloid angiopathy, Icelandic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
Cerebral Infarction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Infarction from the curated CTD Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, App-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, App-Related from the curated CTD Gene-Disease Associations dataset.
Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy from the curated CTD Gene-Disease Associations dataset.
Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.
Infarction, Middle Cerebral Artery Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infarction, Middle Cerebral Artery from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy, Ataxic, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy, Ataxic, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 2 from the curated CTD Gene-Disease Associations dataset.
Diffuse Cerebral Sclerosis of Schilder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diffuse Cerebral Sclerosis of Schilder from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy from the curated CTD Gene-Disease Associations dataset.
Cerebral Cavernous Malformations 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Cavernous Malformations 2 from the curated CTD Gene-Disease Associations dataset.
Hypomyelination, Global Cerebral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypomyelination, Global Cerebral from the curated CTD Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy from the curated CTD Gene-Disease Associations dataset.
Cerebral Cavernous Malformations 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Cavernous Malformations 3 from the curated CTD Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 1 from the curated CTD Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cerebral degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebral degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cerebral arterial disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cerebral arterial disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
cerebral angioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral angioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral primitive neuroectodermal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral sarcoidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral sarcoidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
middle cerebral artery infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease middle cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ataxic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ataxic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral convexity meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral convexity meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral creatine deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral creatine deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
transient cerebral ischemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transient cerebral ischemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spastic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spastic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior cerebral artery infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral neuroblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral neuroblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral arteritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral arteritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral arterial disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral arterial disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral falx meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral falx meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral ventricle cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral ventricle cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dyskinetic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dyskinetic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral lipidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral lipidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral amyloid angiopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral amyloid angiopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria, cerebral; malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set From GAD Gene-Disease Associations genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral cavernous malformations Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral cavernous malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral atherosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarct; stroke, lacunar Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarct; stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; cerebral infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
microangiopathy- related cerebral damage (marcd) Gene Set From GAD Gene-Disease Associations genes associated with the disease microangiopathy- related cerebral damage (marcd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, malaria related; malaria, cerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral palsy; hemiplegia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral palsy; hemiplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, cerebral; malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; cerebral infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral arteriopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral arteriopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral amyloid angiopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral circulation Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral circulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral ischemic events Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral ischemic events in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery diseases; cerebral infarction; Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; cerebral infarction; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; lipoprotein; cerebral infarct Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; lipoprotein; cerebral infarct in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, cerebral; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral palsy; Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral palsy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral small-vessel disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular Gene Set From GAD Gene-Disease Associations genes associated with the disease toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral aging Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral aging in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; cerebral infarction; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; cerebral infarction; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral amyloid angiopathy; senile plaques Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy; senile plaques 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.
malaria; malaria, cerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malarial anemia and cerebral malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease malarial anemia and cerebral malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; intracranial embolism and thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; intracranial embolism and thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral palsy; hemiplegia; virus diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral palsy; hemiplegia; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos Gene Set From GAD Gene-Disease Associations genes associated with the disease diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarct Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarct in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral palsy; pregnancy complications, infectious; virus diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral palsy; pregnancy complications, infectious; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral amyloid angiopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherothrombotic cerebral infarction. Gene Set From GAD Gene-Disease Associations genes associated with the disease atherothrombotic cerebral infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral amyloid angiopathy; plaque, amyloid Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy; plaque, amyloid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarct, atherothrombotic Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarct, atherothrombotic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral arteriopathy; leukoencephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral arteriopathy; leukoencephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; intracranial arteriosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia 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.
cerebral circulation in smokers Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral circulation in smokers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction, atherosclerotic Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction, atherosclerotic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction. Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; hypertension; intracranial arteriosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebral arterial diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebral arterial diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, cerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infarction, middle cerebral artery Gene Set From GAD Gene-Disease Associations genes associated with the disease infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cerebral in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cerebral cortex tangential migration using cell-axon interactions Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex tangential migration using cell-axon interactions biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex tangential migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex regionalization Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex regionalization biological process from the curated GO Biological Process Annotations 2015 dataset.
extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex radially oriented cell migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex radially oriented cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cell motility involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cell motility involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex cell migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
layer formation in cerebral cortex Gene Set From GO Biological Process Annotations 2015 genes participating in the layer formation in cerebral cortex biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of cell motility involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of cell motility involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
substrate-dependent cerebral cortex tangential migration Gene Set From GO Biological Process Annotations 2015 genes participating in the substrate-dependent cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex gabaergic interneuron fate commitment Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex gabaergic interneuron fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex gabaergic interneuron migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex gabaergic interneuron migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebral cortex gabaergic interneuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebral cortex gabaergic interneuron differentiation biological process from the curated GO Biological Process Annotations 2015 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.
cerebral arterial disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cerebral arterial disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of the cerebral subcortex Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of cerebral artery Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb 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.
abnormality of the cerebral vasculature Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature 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.
diffuse cerebral sclerosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the diffuse cerebral sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cerebral ischemia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cerebral ischemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the cerebral cortex Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cerebral aneurysm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cerebral aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cerebral cortex Gene Set From HPA Tissue Protein Expression Profiles proteins with high or low expression in cerebral cortex relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.
small cerebral cortex Gene Set From HPO Gene-Disease Associations genes associated with the small cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral palsy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral aneurysm Gene Set From HPO Gene-Disease Associations genes associated with the cerebral aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.
cerebral venous thrombosis Gene Set From HPO Gene-Disease Associations genes associated with the cerebral venous thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of cerebral artery Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral atrophy 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.
cerebral arteriovenous malformation Gene Set From HPO Gene-Disease Associations genes associated with the cerebral arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral amyloid angiopathy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral amyloid angiopathy 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.
cerebral calcification Gene Set From HPO Gene-Disease Associations genes associated with the cerebral calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral ischemia Gene Set From HPO Gene-Disease Associations genes associated with the cerebral ischemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
arteriosclerosis of small cerebral arteries Gene Set From HPO Gene-Disease Associations genes associated with the arteriosclerosis of small cerebral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcortical cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tortuous cerebral arteries Gene Set From HPO Gene-Disease Associations genes associated with the tortuous cerebral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral vasculitis Gene Set From HPO Gene-Disease Associations genes associated with the cerebral vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased cerebral lipofuscin Gene Set From HPO Gene-Disease Associations genes associated with the increased cerebral lipofuscin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebral vasculature Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebral vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thick cerebral cortex Gene Set From HPO Gene-Disease Associations genes associated with the thick cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral hypomyelination Gene Set From HPO Gene-Disease Associations genes associated with the cerebral hypomyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebral subcortex Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebral subcortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cerebral degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral cortical neurodegeneration Gene Set From HPO Gene-Disease Associations genes associated with the cerebral cortical neurodegeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebral sclerosis Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebral sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebral ventricles Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebral ventricles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral hamartomata Gene Set From HPO Gene-Disease Associations genes associated with the cerebral hamartomata phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neuronal loss in the cerebral cortex Gene Set From HPO Gene-Disease Associations genes associated with the neuronal loss in the cerebral cortex 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.
cerebral cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebral cortex Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral dysmyelination Gene Set From HPO Gene-Disease Associations genes associated with the cerebral dysmyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized cerebral atrophy/hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the cerebral inclusion bodies 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.
frontotemporal cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontotemporal cerebral atrophy 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.
Cerebral Infarction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebral Infarction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Malaria, Cerebral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Malaria, Cerebral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Infarction, Middle Cerebral Artery Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Infarction, Middle Cerebral Artery phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Toxoplasmosis, Cerebral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Toxoplasmosis, Cerebral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebral Arterial Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebral Arterial Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Diffuse Cerebral Sclerosis of Schilder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Diffuse Cerebral Sclerosis of Schilder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dominance, Cerebral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dominance, Cerebral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebral Palsy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebral Palsy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebral Amyloid Angiopathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebral Amyloid Angiopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Infarction, Anterior Cerebral Artery Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Infarction, Anterior Cerebral Artery phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebral Ventricle Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebral Ventricle Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
ectopic cerebral cortex pyramidal cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ectopic cerebral cortex pyramidal cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebral arteriovenous malformation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebral arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebral aqueduct morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebral aqueduct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebral aqueduct Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebral aqueduct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delaminated cerebral cortex Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delaminated cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebral infarction size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin cerebral cortex Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thickened cerebral cortex Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thickened cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebral cortex pyramidal cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebral cortex pyramidal cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebral cortex pyramidal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebral cortex pyramidal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal stratification in cerebral cortex Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal stratification in cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebral cortex morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebral cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebral aqueductal stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebral aqueductal stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebral cortex pyramidal cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebral cortex pyramidal cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cerebral infarction size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{malaria, cerebral, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, cerebral, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral creatine deficiency syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral cavernous malformations 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral cavernous malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral amyloid angiopathy Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral amyloid angiopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, dystonia, and cerebral hypomyelination Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral cavernous malformations-1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral cavernous malformations-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral cavernous malformations-2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral cavernous malformations-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral amyloid angiopathy, dutch, italian, iowa, flemish, arctic variants Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral amyloid angiopathy, dutch, italian, iowa, flemish, arctic variants phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral amyloid angiopathy, prnp-related Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral amyloid angiopathy, prnp-related phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, cerebral, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, cerebral, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral palsy, spastic quadriplegic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral palsy, spastic quadriplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral creatine deficiency syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral creatine deficiency syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination, global cerebral Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination, global cerebral phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral-cerebellar-coloboma syndrome, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral-cerebellar-coloboma syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
{cerebral infarction, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {cerebral infarction, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
neurodegeneration due to cerebral folate transport deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral palsy, spastic quadriplegic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral palsy, spastic quadriplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
vasculopathy, retinal, with cerebral leukodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the vasculopathy, retinal, with cerebral leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral-cortex Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term cerebral-cortex in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
cerebral lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
cerebral hemisphere Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral hemisphere from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
cerebral cortex Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral cortex from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
cerebral lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
cerebral cortex Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral cortex in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
cerebral peduncle Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral peduncle in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
cerebral gyrus Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral gyrus in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
cerebral hemisphere Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cerebral hemisphere in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
right middle cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue right middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
embryonic cerebral cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue embryonic cerebral cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral giant cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral giant cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral gyrus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral gyrus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral granule cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral granule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral peduncle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral peduncle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
middle cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral cortical neuron Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral cortical neuron in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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.
cerebral cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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.
left middle cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue left middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral subcortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral subcortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebral hemisphere Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral hemisphere in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Cerebral Amyloid Angiopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Middle Cerebral Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Middle Cerebral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Cerebral Vasculature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Cerebral Vasculature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Metastasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Metastasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infarction, Middle Cerebral Artery Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infarction, Middle Cerebral Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Adrenoleukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Adrenoleukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Cerebral Sclerosis Of Schilder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Cerebral Sclerosis Of Schilder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Cerebral Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Cerebral Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Artery Atherosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Artery Atherosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Vasospasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Vasospasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination, Global Cerebral Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination, Global Cerebral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cerebral Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cerebral Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Arteriosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Arteriosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cortex Myoclonus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortex Myoclonus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ruptured Cerebral Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, Hereditary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Amyloid Angiopathy, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cortical Hemiatrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Hemiatrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cerebral Amyloid Angiopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcortical Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcortical Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Cerebral Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebral Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Athetoid Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Athetoid Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Palsy, Spastic Quadriplegic, 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Palsy, Spastic Quadriplegic, 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontotemporal Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Cerebral Atrophy/Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Cerebral Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Cerebral Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Middle Cerebral Artery Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Middle Cerebral Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Venous Sinus Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Venous Sinus Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cerebral Hernia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cerebral Hernia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cavernous Malformations 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cavernous Malformations 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Convexity Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Convexity Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Arterial Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Arterial Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Herniation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Herniation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toxoplasmosis, Cerebral Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toxoplasmosis, Cerebral 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.
Cerebral Arterial Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Arterial Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Quadriplegic Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Quadriplegic Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Hypoperfusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Hypoperfusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischaemic Cerebral Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischaemic Cerebral Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Atherosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atherosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sporadic Cerebral Amyloid Angiopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Cerebral Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Cerebral Amyloid Angiopathy, Icelandic Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Abscess Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Abscess in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Diplegia Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Diplegia Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Cerebral Cortex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Cerebral Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thick Cerebral Cortex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thick Cerebral Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Embolism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Embolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Hypoxia-Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Hypoxia-Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Cerebral Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Cerebral Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reversible Cerebral Vasoconstriction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reversible Cerebral Vasoconstriction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Muscular Hypertrophy-Cerebral Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Muscular Hypertrophy-Cerebral Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Cerebral Ventriculomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Cerebral Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cavernous Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cavernous Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cavernous Malformations 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cavernous Malformations 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cavernous Malformations 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cavernous Malformations 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Venous Angioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Venous Angioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Malformation Of Cerebral Vessels Nos Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Of Cerebral Vessels Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cerebral Cavernous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Cavernous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonruptured Congenital Cerebral Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonruptured Congenital Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Malformations Of Cerebral Vessels Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Malformations Of Cerebral Vessels in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts And Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Angiitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Angiitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, Genetic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Amyloid Angiopathy, Genetic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Arteritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Arteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spastic Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spastic Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysgenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysgenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Cerebral Ventricles Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Cerebral Ventricles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonruptured Cerebral Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonruptured Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Primitive Neuroectodermal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Primitive Neuroectodermal Tumor 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.
Cerebral Amyloid Angiopathy, Gsn-Related Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Amyloid Angiopathy, Gsn-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Cerebral Artery Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Cerebral Artery Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Salt-Wasting Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Salt-Wasting Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Arteriopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Arteriopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Volume Loss Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Volume Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malaria, Cerebral, Susceptibility To (Finding) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malaria, Cerebral, Susceptibility To (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thrombosis Of Cerebral Venous Sinus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombosis Of Cerebral Venous Sinus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis, Neurodegeneration, And Cerebral Angiomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis, Neurodegeneration, And Cerebral Angiomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Hygroma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Hygroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Embolism And Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Embolism And Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Thrombus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Thrombus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Monoplegic Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Monoplegic Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Monoplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Monoplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Cerebral Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Cerebral Astrocytoma Of Infancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Cerebral Astrocytoma Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Cerebral, Cerebellar, Coloboma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Cerebral, Cerebellar, Coloboma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Calcification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral Ventriculomegaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dilatation Of The Cerebral Artery Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilatation Of The Cerebral Artery 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 Dysmyelination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Dysmyelination 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.
Cerebral Infarction, Left Hemisphere Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Infarction, Left Hemisphere in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral Infarction, Right Hemisphere Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Infarction, Right Hemisphere in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Embolic Infarction, Middle Cerebral Artery Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Embolic Infarction, Middle Cerebral Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Left Middle Cerebral Artery Infarction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Middle Cerebral Artery Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Middle Cerebral Artery Embolus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Middle Cerebral Artery Embolus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Middle Cerebral Artery Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Middle Cerebral Artery Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Right Middle Cerebral Artery Infarction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Middle Cerebral Artery Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thrombotic Infarction, Middle Cerebral Artery Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thrombotic Infarction, Middle Cerebral Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral Hypomyelination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Hypomyelination 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.
Cerebral Amyloid Angiopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tortuous Cerebral Arteries Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tortuous Cerebral Arteries in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebral Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small Cerebral Cortex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Cerebral Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neuronal Loss In The Cerebral Cortex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In The Cerebral Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anterior Cerebral Circulation Infarction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Cerebral Circulation Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Widened Cerebral Subarachnoid Space Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Cerebral Subarachnoid Space in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Silent Cerebral Infarct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Silent Cerebral Infarct 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.
Ubiquitin-Positive Cerebral Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ubiquitin-Positive Cerebral Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Cerebral Artery Occlusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Cerebral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral Cortical Neurodegeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Cortical Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral Infarction, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Infarction, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Cerebral Lipofuscin Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Cerebral Lipofuscin 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.
cerebral cortex neuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2023 genes participating in the extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebral cortex GABAergic interneuron migration Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex GABAergic interneuron migration biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebral cortex cell migration Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebral cortex GABAergic interneuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex GABAergic interneuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebral cortex tangential migration Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebral cortex radial glia-guided migration Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex radial glia-guided migration biological process from the curated GO Biological Process Annotations 2023 dataset.
pyramidal neuron migration to cerebral cortex Gene Set From GO Biological Process Annotations 2023 genes participating in the pyramidal neuron migration to cerebral cortex biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebral cortex radially oriented cell migration Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex radially oriented cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2023 genes participating in the modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebral cortex GABAergic interneuron development Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebral cortex GABAergic interneuron development biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal cerebral aqueduct morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebral aqueduct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebral cortex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebral cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebral hemisphere morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebral hemisphere morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal stratification in cerebral cortex Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal stratification in cerebral cortex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thickened cerebral cortex Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thickened cerebral cortex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebral cortex pyramidal cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebral cortex pyramidal cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin cerebral cortex Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin cerebral cortex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cerebral infarct size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebral infarct size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebral infarct size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebral infarct size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebral cortex pyramidal cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebral cortex pyramidal cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebral aqueductal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral aqueductal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged cerebral aqueduct Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged cerebral aqueduct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebral blood flow rate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebral blood flow rate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal middle cerebral artery morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal middle cerebral artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebral infarct Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral infarct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebral aqueduct Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebral aqueduct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delaminated cerebral cortex Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delaminated cerebral cortex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebral cortex pyramidal cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral cortex pyramidal cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent segment of posterior cerebral artery Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent segment of posterior cerebral artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent segment of anterior cerebral artery Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent segment of anterior cerebral artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebral arteriovenous malformation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral arteriovenous malformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anastomosis between middle cerebral arteries Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anastomosis between middle cerebral arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal middle cerebral artery origin Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal middle cerebral artery origin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ectopic cerebral cortex pyramidal cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic cerebral cortex pyramidal cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cerebral cortex cell density Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebral cortex cell density phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebral cortex cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebral cortex cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal anterior cerebral artery morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal anterior cerebral artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebral cortex cell density Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebral cortex cell density phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebral cortex average cell area Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebral cortex average cell area phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cerebral cortex cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebral cortex cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Fusiform cerebral cell_Blood vessel_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Fusiform cerebral cell_Blood vessel_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Cerebral organic acidurias including diseases Gene Set From WikiPathways Pathways 2024 proteins participating in the Cerebral organic acidurias including diseases pathway from the WikiPathways Pathways 2024 dataset.
cerebral cortex neuron differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2025 genes participating in the extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebral cortex GABAergic interneuron migration Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex GABAergic interneuron migration biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebral cortex cell migration Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebral cortex GABAergic interneuron differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex GABAergic interneuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebral cortex tangential migration Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebral cortex radial glia-guided migration Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex radial glia-guided migration biological process from the curated GO Biological Process Annotations 2025 dataset.
pyramidal neuron migration to cerebral cortex Gene Set From GO Biological Process Annotations 2025 genes participating in the pyramidal neuron migration to cerebral cortex biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebral cortex radially oriented cell migration Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex radially oriented cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2025 genes participating in the modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebral cortex GABAergic interneuron development Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebral cortex GABAergic interneuron development biological process from the curated GO Biological Process Annotations 2025 dataset.
Cerebral degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
ITM2B-related cerebral amyloid angiopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease ITM2B-related cerebral amyloid angiopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
ITM2B-related cerebral amyloid angiopathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease ITM2B-related cerebral amyloid angiopathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral amyloid angiopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral amyloid angiopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
APP-related cerebral amyloid angiopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease APP-related cerebral amyloid angiopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
CST3-related cerebral amyloid angiopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease CST3-related cerebral amyloid angiopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral folate receptor alpha deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral folate receptor alpha deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral cavernous malformation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral cavernous malformation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral creatine deficiency syndrome 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral arterial disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral arterial disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral arterial disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cerebral arterial disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic quadriplegic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic quadriplegic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ITM2B-related cerebral amyloid angiopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ITM2B-related cerebral amyloid angiopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral cavernous malformation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral cavernous malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ataxic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ataxic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral arterial disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral arterial disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral creatine deficiency syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral creatine deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral amyloid angiopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral amyloid angiopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
APP-related cerebral amyloid angiopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease APP-related cerebral amyloid angiopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral ventricle cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral ventricle cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient cerebral ischemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient cerebral ischemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral arteritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral arteritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vasculopathy with cerebral leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vasculopathy with cerebral leukodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ITM2B-related cerebral amyloid angiopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease ITM2B-related cerebral amyloid angiopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
CST3-related cerebral amyloid angiopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease CST3-related cerebral amyloid angiopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dyskinetic cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dyskinetic cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Middle cerebral artery infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Middle cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral falx meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral falx meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior cerebral artery infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anterior cerebral artery infarction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anterior cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral angioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral angioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral convexity meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral convexity meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral folate receptor alpha deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral folate receptor alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral neuroblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral neuroblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
deafness, dystonia, and cerebral hypomyelination Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease deafness, dystonia, and cerebral hypomyelination in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral hemisphere lipoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral hemisphere lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral primitive neuroectodermal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral lipidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral lipidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic quadriplegic cerebral palsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic quadriplegic cerebral palsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral cortex Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral cortex from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral hemisphere Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral hemisphere from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral lobe Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral hemisphere Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral hemisphere in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral cortex Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral cortex in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral lobe Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral gyrus Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral gyrus in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral peduncle Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cerebral peduncle in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral hemisphere Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral hemisphere in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression 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.
Cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Middle cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral cortical neuron Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral cortical neuron in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 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.
Cerebral gyrus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral gyrus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Left middle cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Left middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Right middle cerebral artery Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Right middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral subcortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral subcortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral peduncle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral peduncle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Embryonic cerebral cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Embryonic cerebral cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral giant cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral giant cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral granule cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral granule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebral palsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral palsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral cavernous malformation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cavernous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary cerebral amyloid angiopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary cerebral amyloid angiopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HTRA1-related cerebral small vessel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HTRA1-related cerebral small vessel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral arteriopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral arteriopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral creatine deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral creatine deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral dysmyelination Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral dysmyelination phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal cerebral morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal cerebral morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral arteriovenous malformation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CEREBRAL CAVERNOUS MALFORMATIONS Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CEREBRAL CAVERNOUS MALFORMATIONS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral folate transport deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral folate transport deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral amyloid angiopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral amyloid angiopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral autosomal dominant arteriopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral autosomal dominant arteriopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral calcification Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral calcification phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral visual impairment and intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral visual impairment and intellectual disability 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.
Cerebral small vessel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral small vessel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dilatation of the cerebral artery Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dilatation of the cerebral artery phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral cortical atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cortical atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral arterial disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral arterial disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atypical cerebral palsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical cerebral palsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
COL4A1 or COL4A2-related cerebral small vessel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the COL4A1 or COL4A2-related cerebral small vessel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal cerebral cortex morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal cerebral cortex morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic cerebral palsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic cerebral palsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Harmonizome 3.0

brain edema; cerebral hemorrhage; Gene Set

brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene Set

apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage Gene Set

apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set

cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension Gene Set

brain edema; brain hemorrhage, traumatic Gene Set

cerebral hemorrhage; cerebral hemorrhages; cerebral infarction Gene Set

cerebral amyloid angiopathy; cerebral hemorrhage; cerebral hemorrhages Gene Set

cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular Gene Set

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke Gene Set

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene Set

cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension Gene Set

cerebral hemorrhage; cerebral infarction; stroke Gene Set

cerebral hemorrhage; cerebral hemorrhages; dementia, vascular Gene Set

amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set

cerebral hemorrhage; cerebral hemorrhages; hypertension Gene Set

cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis Gene Set

cerebral hemorrhage; cerebral hemorrhages Gene Set

cerebral hemorrhage; cerebral hemorrhages; memory disorders Gene Set

brain edema; infarction, middle cerebral artery Gene Set

aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke Gene Set

brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage Gene Set

brain ischemia; cerebral hemorrhage; stroke Gene Set

brain infarction; cadasil; cerebral hemorrhage; Gene Set

brain edema; brain injuries Gene Set

gastrointestinal diseases; gastrointestinal hemorrhage; peptic ulcer; peptic ulcer hemorrhage Gene Set

cerebral edema Gene Set

cerebral edema Gene Set

High Altitude Cerebral Edema Gene Set

Fulminant Hepatic Failure With Cerebral Edema Gene Set

Cerebral Edema Gene Set

Cytotoxic Cerebral Edema Gene Set

Vasogenic Cerebral Edema Gene Set

cerebral edema Gene Set

brain concussion; brain injuries; brain ischemia Gene Set

Cerebral hemorrhage with amyloidosis, hereditary, Dutch type Gene Set

Cerebral Hemorrhage Gene Set

cerebral amyloid angiopathy-related hemorrhage. Gene Set

cerebral infarction; memory disorders; subarachnoid hemorrhage Gene Set

cerebral hemorrhage; Gene Set

cerebral hemorrhage; stroke Gene Set

cerebral hemorrhage; intracranial arteriovenous malformations Gene Set

cerebral hemorrhage Gene Set

cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke Gene Set

cerebral hemorrhage; leukomalacia, periventricular; sepsis Gene Set

cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia Gene Set

cerebral hemorrhage; recurrence; stroke Gene Set

recurrent cerebral hemorrhage Gene Set

cerebral hemorrhage Gene Set

Cerebral Hemorrhage, Traumatic Gene Set

Cerebral Hemorrhage Gene Set

Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type Gene Set

Recurrent Cerebral Hemorrhage Gene Set

Cerebral Hemorrhage Gene Set

Fetal akinesia-cerebral and retinal hemorrhage syndrome Gene Set

Brain Edema Gene Set

brain edema Gene Set

Brain Edema Gene Set

Brain Edema Gene Set

Cytotoxic Brain Edema Gene Set

Vasogenic Brain Edema Gene Set

Brain edema Gene Set

Brain small vessel disease with hemorrhage Gene Set

Brain Small Vessel Disease with Hemorrhage Gene Set

brain hemorrhage Gene Set

brain ischemia; subarachnoid hemorrhage Gene Set

brain hemorrhage; stroke, ischemic Gene Set

brain hemorrhage; cerebrovascular disease; thrombosis, deep vein Gene Set

brain ischemia; hemorrhage Gene Set

brain ischemia; subarachnoid hemorrhage; vasospasm, intracranial Gene Set

apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set

brain hemorrhage; stroke; stroke, lacunar Gene Set

Brain Hemorrhage, Traumatic Gene Set

{intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} Gene Set

Brain Hemorrhage Gene Set

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set

cerebral infarct; cerebral arteriopathy Gene Set

apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set

brain infarction; cerebral arterial diseases Gene Set