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Parent Node:
expandAmnesia (D000647)
Parent Node:
expandBrain Diseases (D001927)
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..expandAmnesia, Transient Global (D020236)

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 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
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..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
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..expandHypothalamic Diseases (D007027) Child80
..expandHypoxia, Brain (D002534) Child2
..expandIntracranial Hypertension (D019586) Child57
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..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:557
Name:Amnesia, Transient Global
Definition:A syndrome characterized by a transient loss of the ability to form new memories. It primarily occurs in middle aged or elderly individuals, and episodes may last from minutes to hours. During the period of amnesia, immediate and recent memory abilities are impaired, but the level of consciousness and ability to perform other intellectual tasks are preserved. The condition is related to bilateral dysfunction of the medial portions of each TEMPORAL LOBE. Complete recovery normally occurs, and recurrences are unusual. (From Adams et al., Principles of Neurology, 6th ed, pp429-30)
Alternative IDs:
ParentIDs:MESH:D000647|MESH:D001927
TreeNumbers:C10.228.140.060 |C10.597.606.525.100.800 |C23.888.592.604.529.100.800 |F03.087.200.800
Synonyms:Global Amnesia, Transient |TGAs (Transient Global Amnesia) |TGA (Transient Global Amnesia) |Transient Global Amnesia
Slim Mappings:Mental disorder|Nervous system disease|Signs and symptoms
Reference: MedGen: D020236
MeSH: D020236
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants