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Disease Browser
Parent Node:
expandEpilepsy (D004827)
..Starting node
..expandEpilepsies, Partial (D004828)

       Child Nodes:
........expandCortical Dysplasia-Focal Epilepsy Syndrome (C566482)
........expandEpilepsy, Complex Partial (D017029)
........expandEpilepsy, Frontal Lobe (D017034) Child6
........expandEpilepsy, Partial, Motor (D020938)
........expandEpilepsy, Partial, Sensory (D020937) Child1
........expandEpilepsy, Partial, with Pericentral Spikes (C564605)
........expandEpilepsy, Partial, with Variable Foci (C565785)
........expandEpilepsy, Rolandic (D019305) Child3
........expandEpilepsy, Temporal Lobe (D004833) Child6
........expandPitt-Hopkins-Like Syndrome 1 (C567657)



 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:3851
Name:Epilepsies, Partial
Definition:Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into simple and complex, depending on whether consciousness is unaltered (simple partial seizure) or disturbed (complex partial seizure). Both types may feature a wide variety of motor, sensory, and autonomic symptoms. Partial seizures may be classified by associated clinical features or anatomic location of the seizure focus. A secondary generalized seizure refers to a partial seizure that spreads to involve the brain diffusely. (From Adams et al., Principles of Neurology, 6th ed, pp317)
Alternative IDs:
ParentIDs:MESH:D004827
TreeNumbers:C10.228.140.490.360
Synonyms:Abdominal Epilepsies |Abdominal Epilepsy |Amygdalo-Hippocampal Epilepsies |Amygdalo-Hippocampal Epilepsy |Benign Focal Epilepsy, Childhood |Benign Occipital Epilepsies |Benign Occipital Epilepsy |Benign Occipital Epilepsy, Childhood |Childhood Benign Focal Epile
Slim Mappings:Nervous system disease
Reference: MedGen: D004828
MeSH: D004828
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants