Encephalopathy, Acute, Infection-Induced, Susceptibility To, 3 |
|
Gliosis, Cerebral edema |
OMIM:608033 |
Encephalopathy, Acute, Infection-Induced, Susceptibility To, 4 |
|
Cerebral edema |
OMIM:614212 |
Glioblastoma |
|
Abnormal cerebral white matter morphology, Cerebral edema, Abnormal corpus callosum morphology |
ORPHA:360 |
Kcnq2-Related Epileptic Encephalopathy |
|
Abnormal globus pallidus morphology, Cerebral atrophy, Abnormal cerebral white matter morphology,... |
ORPHA:439218 |
Focal Cortical Dysplasia, Type Ii |
|
Cortical dysplasia, Focal cortical dysplasia type II, Hemimegalencephaly, Astrocytosis, Focal whi... |
OMIM:607341 |
Familial Acute Necrotizing Encephalopathy |
|
Abnormal putamen morphology, Gliosis, Cerebral edema |
ORPHA:88619 |
Neurodevelopmental Disorder With Microcephaly, Hypotonia, Nystagmus, And Seizures |
|
Corpus callosum atrophy, Cerebral edema, Cerebral atrophy, Microcephaly |
OMIM:619876 |
Hyperglycinemia, Lactic Acidosis, And Seizures |
|
Cerebral edema, Cerebral atrophy, Microcephaly |
OMIM:614462 |
Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due To |
|
Cerebral edema |
OMIM:237300 |
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of |
|
Cerebral edema |
OMIM:201450 |
Alzheimer Disease, Familial Early-Onset, With Coexisting Amyloid And Prion Pathology |
|
Neurofibrillary tangles, Cerebral cortex with spongiform changes |
OMIM:605055 |
Maple Syrup Urine Disease |
|
Cerebral edema |
OMIM:248600 |
Early-onset Alzheimer disease with cerebral amyloid angiopathy |
|
Neurofibrillary tangles |
DECIPHER:48 |
Alzheimer Disease 2 |
|
Neurofibrillary tangles |
OMIM:104310 |
Encephalopathy, Progressive, Early-Onset, With Brain Edema And/Or Leukoencephalopathy, 2 |
|
Abnormal cerebral white matter morphology, Gliosis, Cerebral edema, Cerebral atrophy |
OMIM:618321 |
Reversible Cerebral Vasoconstriction Syndrome |
|
Ischemic stroke, Cerebral edema, Leukoencephalopathy |
ORPHA:284388 |
Citrullinemia, Type Ii, Adult-Onset |
|
Cerebral edema |
OMIM:603471 |
Steroid-Responsive Encephalopathy Associated With Autoimmune Thyroiditis |
|
Abnormal cerebral white matter morphology, Cerebral edema |
ORPHA:83601 |
Spongiform Encephalopathy With Neuropsychiatric Features |
|
Neurofibrillary tangles, Cerebral cortex with spongiform changes, Gliosis |
OMIM:606688 |
Encephalopathy, Progressive, Early-Onset, With Brain Edema And/Or Leukoencephalopathy, 1 |
|
Cerebral white matter atrophy, Cerebral edema, Leukoencephalopathy |
OMIM:617186 |
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 8 |
|
Neurofibrillary tangles, Amyotrophic lateral sclerosis |
OMIM:619132 |
Mitochondrial Complex I Deficiency, Nuclear Type 20 |
|
Cerebral edema |
OMIM:611126 |
Migraine, Familial Hemiplegic, 2 |
|
Cerebral edema |
OMIM:602481 |
Acute Disseminated Encephalomyelitis |
|
Hypointensity of cerebral white matter on MRI, Diffuse white matter abnormalities, Abnormal basal... |
ORPHA:83597 |
Herpes Simplex Virus Encephalitis |
|
Cerebral edema |
ORPHA:1930 |
Combined Oxidative Phosphorylation Deficiency 33 |
|
Cerebral edema, Oligohydramnios |
OMIM:617713 |
Alzheimer Disease, Familial, 1 |
|
Neurofibrillary tangles |
OMIM:104300 |
Acyl-Coa Dehydrogenase 9 Deficiency |
|
Cerebral edema |
ORPHA:99901 |
Dural Sinus Malformation |
|
Hypoplasia of the frontal lobes, Cerebral edema |
ORPHA:97339 |
Japanese Encephalitis |
|
Abnormal substantia nigra morphology, Abnormal caudate nucleus morphology, Abnormal cerebral morp... |
ORPHA:79139 |
Laminin Subunit Alpha 2-Related Congenital Muscular Dystrophy |
|
Pachygyria, Lissencephaly, Cerebral edema, Astrocytosis |
ORPHA:258 |
Mitochondrial Complex Iv Deficiency, Nuclear Type 22 |
|
Cerebral edema |
OMIM:619355 |
Angiostrongyliasis |
|
Cerebral edema |
ORPHA:74 |
Familial Or Sporadic Hemiplegic Migraine |
|
Cerebral edema |
ORPHA:569 |
Lujo Hemorrhagic Fever |
|
Facial edema, Periorbital edema, Cerebral edema, Generalized edema |
ORPHA:319213 |
Alzheimer Disease 9, Susceptibility To |
|
Neurofibrillary tangles, Hippocampal atrophy, Cerebral cortical atrophy |
OMIM:608907 |
Citrullinemia Type Ii |
|
Cerebral edema |
ORPHA:247585 |
Citrullinemia, Classic |
|
Cerebral edema |
OMIM:215700 |
Amoebiasis Due To Free-Living Amoebae |
|
Abnormal basal ganglia morphology, Abnormal cerebral white matter morphology, Encephalomalacia, A... |
ORPHA:68 |
Ethylene Glycol Poisoning |
|
Cerebral edema, Pulmonary edema |
ORPHA:31826 |
Mitochondrial Complex I Deficiency, Nuclear Type 1 |
|
Microcephaly, Focal T2 hypointense basal ganglia lesion, Leukoencephalopathy, Focal T2 hyperinten... |
OMIM:252010 |
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To |
|
Cerebral edema |
OMIM:311250 |
Megalencephalic Leukoencephalopathy With Subcortical Cysts 2B, Remitting, With Or Without Impaired Intellectual Development |
|
Diffuse swelling of cerebral white matter, Diffuse white matter abnormalities, Megalencephaly |
OMIM:613926 |
Cryptococcosis |
|
Pleural effusion, Cerebral cortical atrophy, Cerebral edema |
ORPHA:1546 |
Progressive Non-Fluent Aphasia |
|
Neurofibrillary tangles, Temporal cortical atrophy, Astrocytosis, Frontotemporal cerebral atrophy... |
ORPHA:100070 |
Argininosuccinic Aciduria |
|
Cerebral edema |
OMIM:207900 |
X-Linked Intellectual Disability, Snyder Type |
|
Cerebral edema, Megalencephaly |
ORPHA:3063 |
Frontotemporal Lobar Degeneration With Tdp43 Inclusions, Grn-Related |
|
Neurofibrillary tangles, Lewy bodies, Gliosis, Cerebral cortical atrophy |
OMIM:607485 |
Parkinson Disease 23, Autosomal Recessive Early-Onset |
|
Neurofibrillary tangles, Lewy bodies, Cerebral cortical atrophy |
OMIM:616840 |
Acute Liver Failure |
|
Cerebral edema |
ORPHA:90062 |
Alzheimer Disease 3 |
|
Neurofibrillary tangles, Cerebral cortical atrophy |
OMIM:607822 |
Supranuclear Palsy, Progressive, 1 |
|
Neuronal loss in basal ganglia, Neurofibrillary tangles, Cerebral atrophy, Granulovacuolar degene... |
OMIM:601104 |
Alzheimer Disease 4 |
|
Neurofibrillary tangles |
OMIM:606889 |
Early-Onset Autosomal Dominant Alzheimer Disease |
|
Neurofibrillary tangles, Cerebral cortical atrophy |
ORPHA:1020 |
Supranuclear Palsy, Progressive, 2 |
|
Neurofibrillary tangles, Neuronal loss in basal ganglia, Gliosis, Granulovacuolar degeneration |
OMIM:609454 |
Cerebral Amyloid Angiopathy, Itm2B-Related, 2 |
|
Neurofibrillary tangles |
OMIM:117300 |
Niemann-Pick Disease, Type C1 |
|
Neurofibrillary tangles, Fetal ascites |
OMIM:257220 |
Niemann-Pick Disease, Type C2 |
|
Neurofibrillary tangles, Fetal ascites, Polyhydramnios |
OMIM:607625 |
Neurodegeneration With Brain Iron Accumulation 2B |
|
Neurofibrillary tangles, Lewy bodies, Cerebral atrophy |
OMIM:610217 |
Gerstmann-Straussler Disease |
|
Neurofibrillary tangles |
OMIM:137440 |
Adult-Onset Dystonia-Parkinsonism |
|
Neurofibrillary tangles, Frontotemporal cerebral atrophy, Generalized cerebral atrophy/hypoplasia |
ORPHA:199351 |
Megalencephalic Leukoencephalopathy With Subcortical Cysts 2A |
|
Diffuse swelling of cerebral white matter, Diffuse white matter abnormalities, Cerebral atrophy, ... |
OMIM:613925 |
Macrocephaly-Intellectual Disability-Autism Syndrome |
|
|
ORPHA:210548 |