Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandEpilepsy (D004827)
..Starting node
..expandEpilepsy, Reflex (D020195)

       Child Nodes:



 Sister Nodes: 
..expandAICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency (C563876)
..expandAlopecia epilepsy oligophrenia syndrome of Moynahan (C537052)
..expandAlopecia, epilepsy, pyorrhea, mental subnormality (C537057)
..expandAmish Infantile Epilepsy Syndrome (C563799)
..expandArthrogryposis epileptic seizures migrational brain disorder (C537442)
..expandBattaglia Neri syndrome (C537662)
..expandBETA-AMINO ACIDS, RENAL TRANSPORT OF (OMIM:109660)
..expandBorjeson-Forssman-Lehmann syndrome (C536575)
..expandBoudhina Yedes Khiari syndrome (C537939)
..expandCHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB (OMIM:613729)
..expandCoffin syndrome 1 (C536435)
..expandDevelopmental Delay, Epilepsy, and Neonatal Diabetes (C565253)
..expandEpilepsies, Myoclonic (D004831) Child26
..expandEpilepsies, Partial (D004828) Child26
..expandEpilepsy occipital calcifications (C535496)
..expandEpilepsy telangiectasia (C535497)
..expandEpilepsy, Benign Neonatal (D020936) Child13
..expandEpilepsy, Benign Neonatal, 1, And/Or Myokymia (C567743)
..expandEpilepsy, Female-Restricted, with Mental Retardation (C564715)
..expandEpilepsy, Generalized (D004829) Child27
..expandEPILEPSY, HOT WATER, 1 (OMIM:613339)
..expandEPILEPSY, HOT WATER, 2 (OMIM:613340)
..expandEpilepsy, Photogenic, with Spastic Diplegia and Mental Retardation (C565587)
..expandEpilepsy, Post-Traumatic (D004834)
..expandEpilepsy, Reflex (D020195)
..expandEpilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders (C564505)
..expandFryns-Aftimos Syndrome (C565258)
..expandGurrieri Sammito Bellussi syndrome (C537625)
..expandHETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT (OMIM:300049)
..expandHyperekplexia and Epilepsy (C564474)
..expandKifafa seizure disorder (C537708)
..expandKohlschutter Tonz syndrome (C537213)
..expandKuzniecky syndrome (C538091)
..expandLandau-Kleffner Syndrome (D018887)
..expandLennox Gastaut Syndrome (D065768) Child1
..expandMEHMO syndrome (C537451)
..expandMENTAL RETARDATION, AUTOSOMAL DOMINANT 20 (OMIM:613443)
..expandMental Retardation, Microcephaly, Epilepsy, And Coarse Face (C563342)
..expandMental Retardation, X-Linked, Syndromic, Christianson Type (C567484)
..expandMental Retardation, X-Linked, with Epilepsy (C564516)
..expandPolyhydramnios, Megalencephaly, And Symptomatic Epilepsy (C567020)
..expandPyridoxine-dependent epilepsy (C536254)
..expandRamon Syndrome (C535285)
..expandRetinal Degeneration and Epilepsy (C564847)
..expandRud Syndrome (C535878)
..expandSandhaus Ben-Ami syndrome (C537233)
..expandSeizures (D012640) Child40
..expandSeizures, Febrile (D003294) Child21
..expandSpinocerebellar Ataxia with Epilepsy (C564395)
..expandStatus Epilepticus (D013226) Child1
..expandWittwer syndrome (C536737)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:3894
Name:Epilepsy, Reflex
Definition:A subtype of epilepsy characterized by seizures that are consistently provoked by a certain specific stimulus. Auditory, visual, and somatosensory stimuli as well as the acts of writing, reading, eating, and decision making are examples of events or activities that may induce seizure activity in affected individuals. (From Neurol Clin 1994 Feb;12(1):57-8)
Alternative IDs:
ParentIDs:MESH:D004827
TreeNumbers:C10.228.140.490.450
Synonyms:Audiogenic Epilepsies |Audiogenic Epilepsy |Audiogenic Reflex Epilepsies |Audiogenic Reflex Epilepsy |Cursive Epilepsy |Cursive Reflex Epilepsies (Running) |Cursive Reflex Epilepsy (Running) |Decision Making Reflex Epilepsy |Eating-Induced Epilepsies |Eating Indu
Slim Mappings:Nervous system disease
Reference: MedGen: D020195
MeSH: D020195
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants