Disease Browser
Parent Node: Brain Injuries (D001930) Parent Node: Epilepsy (D004827) ..Starting node .. Epilepsy, Post-Traumatic (D004834) Child Nodes:
Sister Nodes: ..AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency (C563876) ..Alopecia epilepsy oligophrenia syndrome of Moynahan (C537052) ..Alopecia, epilepsy, pyorrhea, mental subnormality (C537057) ..Amish Infantile Epilepsy Syndrome (C563799) ..Arthrogryposis epileptic seizures migrational brain disorder (C537442) ..Battaglia Neri syndrome (C537662) ..BETA-AMINO ACIDS, RENAL TRANSPORT OF (OMIM:109660) ..Borjeson-Forssman-Lehmann syndrome (C536575) ..Boudhina Yedes Khiari syndrome (C537939) ..CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB (OMIM:613729) ..Coffin syndrome 1 (C536435) ..Developmental Delay, Epilepsy, and Neonatal Diabetes (C565253) ..Epilepsies, Myoclonic (D004831) 26 ..Epilepsies, Partial (D004828) 26 ..Epilepsy occipital calcifications (C535496) ..Epilepsy telangiectasia (C535497) ..Epilepsy, Benign Neonatal (D020936) 13 ..Epilepsy, Benign Neonatal, 1, And/Or Myokymia (C567743) ..Epilepsy, Female-Restricted, with Mental Retardation (C564715) ..Epilepsy, Generalized (D004829) 27 ..EPILEPSY, HOT WATER, 1 (OMIM:613339) ..EPILEPSY, HOT WATER, 2 (OMIM:613340) ..Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation (C565587) ..Epilepsy, Post-Traumatic (D004834) ..Epilepsy, Reflex (D020195) ..Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders (C564505) ..Fryns-Aftimos Syndrome (C565258) ..Gurrieri Sammito Bellussi syndrome (C537625) ..HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT (OMIM:300049) ..Hyperekplexia and Epilepsy (C564474) ..Kifafa seizure disorder (C537708) ..Kohlschutter Tonz syndrome (C537213) ..Kuzniecky syndrome (C538091) ..Landau-Kleffner Syndrome (D018887) ..Lennox Gastaut Syndrome (D065768) 1 ..MEHMO syndrome (C537451) ..MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 (OMIM:613443) ..Mental Retardation, Microcephaly, Epilepsy, And Coarse Face (C563342) ..Mental Retardation, X-Linked, Syndromic, Christianson Type (C567484) ..Mental Retardation, X-Linked, with Epilepsy (C564516) ..Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy (C567020) ..Pyridoxine-dependent epilepsy (C536254) ..Ramon Syndrome (C535285) ..Retinal Degeneration and Epilepsy (C564847) ..Rud Syndrome (C535878) ..Sandhaus Ben-Ami syndrome (C537233) ..Seizures (D012640) 40 ..Seizures, Febrile (D003294) 21 ..Spinocerebellar Ataxia with Epilepsy (C564395) ..Status Epilepticus (D013226) 1 ..Wittwer syndrome (C536737) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 3888
Name: Epilepsy, Post-Traumatic
Definition: Recurrent seizures causally related to CRANIOCEREBRAL TRAUMA. Seizure onset may be immediate but is typically delayed for several days after the injury and may not occur for up to two years. The majority of seizures have a focal onset that correlates clinically with the site of brain injury. Cerebral cortex injuries caused by a penetrating foreign object (CRANIOCEREBRAL TRAUMA, PENETRATING) are more likely than closed head injuries (HEAD INJURIES, CLOSED) to be associated with epilepsy. Concussive convulsions are nonepileptic phenomena that occur immediately after head injury and are characterized by tonic and clonic movements. (From Rev Neurol 1998 Feb;26(150):256-261; Sports Med 1998 Feb;25(2):131-6)
Alternative IDs:
ParentIDs: MESH:D001930|MESH:D004827
TreeNumbers: C10.228.140.199.650 |C10.228.140.490.380 |C10.900.300.087.600 |C26.260.118.475 |C26.915.300.200.475
Synonyms: Concussive Convulsion |Concussive Convulsions |Convulsion, Concussive |Convulsions, Concussive |Disorder, Post-Traumatic Seizure |Disorders, Post-Traumatic Seizure |Early Post-Traumatic Seizure |Early Post Traumatic Seizures |Early Post-Traumatic Seizures |Epilep
Slim Mappings: Nervous system disease|Wounds and injuries
Reference:
MedGen: D004834
MeSH: D004834
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants