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:
expandEpilepsy (D004827)
..Starting node
..expandSeizures, Febrile (D003294)

       Child Nodes:
........expandFebrile Convulsions, Familial, 1 (C565162)
........expandFebrile Convulsions, Familial, 10 (C567218)
........expandFebrile Convulsions, Familial, 2 (C566541)
........expandFebrile Convulsions, Familial, 3a (C567820)
........expandFebrile Convulsions, Familial, 3b (C567821)
........expandFebrile Convulsions, Familial, 4 (C565788)
........expandFebrile Convulsions, Familial, 5 (C563762)
........expandFebrile Convulsions, Familial, 6 (C563764)
........expandFebrile Convulsions, Familial, 7 (C566929)
........expandFebrile Convulsions, Familial, 8 (C566975)
........expandFebrile Convulsions, Familial, 9 (C566901)
........expandFebrile Seizures Associated with Afebrile Seizures (C565813)
........expandGeneralized Epilepsy with Febrile Seizures Plus (C565808)
........expandGeneralized Epilepsy With Febrile Seizures Plus, 7 (C567827)
........expandGeneralized Epilepsy With Febrile Seizures Plus, Type 1 (C565809)
........expandGeneralized Epilepsy With Febrile Seizures Plus, Type 2 (C565810)
........expandGeneralized Epilepsy With Febrile Seizures Plus, Type 3 (C565811)
........expandGeneralized Epilepsy With Febrile Seizures Plus, Type 4 (C565227)
........expandGeneralized Epilepsy With Febrile Seizures Plus, Type 5 (C565812)
........expandGeneralized Epilepsy With Febrile Seizures Plus, Type 6 (C567371)
........expandGENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8 (OMIM:613828)



 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:10112
Name:Seizures, Febrile
Definition:Seizures that occur during a febrile episode. It is a common condition, affecting 2-5% of children aged 3 months to five years. An autosomal dominant pattern of inheritance has been identified in some families. The majority are simple febrile seizures (generally defined as generalized onset, single seizures with a duration of less than 30 minutes). Complex febrile seizures are characterized by focal onset, duration greater than 30 minutes, and/or more than one seizure in a 24 hour period. The likelihood of developing epilepsy (i.e., a nonfebrile seizure disorder) following simple febrile seizures is low. Complex febrile seizures are associated with a moderately increased incidence of epilepsy. (From Menkes, Textbook of Child Neurology, 5th ed, p784)
Alternative IDs:
ParentIDs:MESH:D004827
TreeNumbers:C10.228.140.490.650
Synonyms:Convulsion, Febrile |Convulsion, Fever |Convulsion, Pyrexial |Convulsions, Febrile |Convulsions, Fever |Convulsions, Pyrexial |Febrile Convulsion |Febrile Convulsions |Febrile Convulsion Seizure |Febrile Convulsion Seizures |Febrile Fit |Febrile Fits |Febrile Seizur
Slim Mappings:Nervous system disease
Reference: MedGen: D003294
MeSH: D003294
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants