Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandBrain Diseases (D001927)
..Starting node
..expandBrain Edema (D001929)

       Child Nodes:
........expandPEHO syndrome (C536317)



 Sister Nodes: 
..expandAkinetic Mutism (D000405)
..expandAmblyopia (D000550) Child2
..expandAmnesia, Transient Global (D020236)
..expandAuditory Diseases, Central (D001304) Child19
..expandBaraitser Brett Piesowicz syndrome (C537905)
..expandBasal Ganglia Diseases (D001480) Child102
..expandBeta-Ureidopropionase Deficiency (C563210)
..expandBrain Abscess (D001922) Child1
..expandBrain Damage, Chronic (D001925) Child13
..expandBrain Death (D001926)
..expandBrain Diseases, Metabolic (D001928) Child244
..expandBrain Edema (D001929) Child1
..expandBrain Injuries (D001930) Child11
..expandBrain Neoplasms (D001932) Child30
..expandCerebellar Diseases (D002526) Child162
..expandCerebrovascular Disorders (D002561) Child108
..expandColpocephaly (C535973)
..expandCrome syndrome (C536216)
..expandDementia (D003704) Child73
..expandDermatoleukodystrophy (C538220)
..expandDiffuse Cerebral Sclerosis of Schilder (D002549) Child3
..expandEncephalitis (D004660) Child32
..expandEncephalomalacia (D004678) Child2
..expandEpilepsy (D004827) Child196
..expandGranulomas, congenital cerebral (C537294)
..expandHashimoto's encephalitis (C535841)
..expandHeadache Disorders (D020773) Child26
..expandHydrocephalus (D006849) Child52
..expandHypothalamic Diseases (D007027) Child80
..expandHypoxia, Brain (D002534) Child2
..expandIntracranial Hypertension (D019586) Child57
..expandIntracranial Hypotension (D019585)
..expandKeratosis follicularis dwarfism cerebral atrophy (C536158)
..expandKluver-Bucy Syndrome (D020232) Child1
..expandLeukoencephalopathies (D056784) Child70
..expandMacrogyria, pseudobulbar palsy and mental retardation (C537722)
..expandMICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY (OMIM:613668)
..expandNeu Laxova syndrome (C536405)
..expandNeuroaxonal Dystrophies (D019150) Child13
..expandNon-lissencephalic cortical dysplasia (C536243)
..expandRAJAB SYNDROME (OMIM:613658)
..expandRambaud Galian syndrome (C535283)
..expandSener syndrome (C537579)
..expandSepsis-Associated Encephalopathy (D065166)
..expandSpastic Pseudosclerosis (C563024)
..expandSubdural Effusion (D013353)
..expandThalamic Diseases (D013786) Child1
..expandThyrocerebral-retinal syndrome (C536908)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1449
Name:Brain Edema
Definition:Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6)
Alternative IDs:
ParentIDs:MESH:D001927
TreeNumbers:C10.228.140.187
Synonyms:Brain Edema, Cytotoxic |Brain Edema, Vasogenic |Brain Swelling |Brain Swellings |Cerebral Edema |Cerebral Edema, Cytotoxic |Cerebral Edemas, Vasogenic |Cerebral Edema, Vasogenic |Cytotoxic Brain Edema |Cytotoxic Cerebral Edema |Edema, Brain |Edema, Cerebral |Edema,
Slim Mappings:Nervous system disease
Reference: MedGen: D001929
MeSH: D001929
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants