Other generalized epilepsy and epileptic syndromes

Preferred Label : Other generalized epilepsy and epileptic syndromes;

Inclusion CIM-10 : Nonspecific clonic epileptic seizures; Grand mal seizure NOS; Nonspecific tonic-clonic epileptic seizures; Nonspecific tonic epileptic seizures; Nonspecific myoclonic epileptic seizures; Epilepsy with myoclonic absences; Epilepsy with myoclonic-astatic seizures; Nonspecific atonic epileptic seizures; Epilepsy with grand mal seizures on awakening; Symptomatic early myoclonic encephalopathy;

Diag associé à un acte (%) : 81.4;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

G404;

UMLS CUI

C0477370;

Automatic exact mappings (from CISMeF team)
- Early myoclonic encephalopathy (disorder) [SNOMED CT concept]
- Epilepsy with generalized tonic-clonic seizures alone (disorder) [SNOMED CT concept]
- Epilepsy with myoclonic absence (disorder) [SNOMED CT concept]
- Epilepsy with myoclonic-astatic seizures [ICD-11 Sub-sub category]
- Lennox Gastaut Syndrome [MeSH Descriptor]
- Lennox Gastaut Syndrome [MeSH concept]
- Lennox-Gastaut Syndrome [NCIt concept]
- Myoclonic-astatic epilepsy [ORDO Disease]
- West Syndrome [NCIt concept]
- epilepsies, myoclonic [MeSH Descriptor]
- spasms, infantile [MeSH Descriptor]
- spasms, infantile [MeSH concept]
Excluded by
- Cramp and spasm [ICD-10 Sub-category]
Orphanet concepts
- Action myoclonus-renal failure syndrome [ORDO Disease]
- Acute encephalopathy with biphasic seizures and late reduced diffusion [ORDO Disease]
- Adolescent-onset epilepsy syndrome [ORDO Disease]
- Benign familial neonatal-infantile seizures [ORDO Disease]
- Benign idiopathic neonatal seizures [ORDO Disease]
- Benign infantile seizures associated with mild gastroenteritis [ORDO Disease]
- Benign non-familial infantile seizures [ORDO Disease]
- CDKL5-deficiency disorder [ORDO Disease]
- Childhood encephalopathy due to thiamine pyrophosphokinase deficiency [ORDO Disease]
- Childhood-onset epilepsy syndrome [ORDO Disease]
- Classic glucose transporter type 1 deficiency syndrome [ORDO Disease]
- Continuous spikes and waves during sleep [ORDO Disease]
- Cryptogenic late-onset epileptic spasms [ORDO Disease]
- Dravet syndrome [ORDO Disease]
- EAST syndrome [ORDO Disease]
- Early myoclonic encephalopathy [ORDO Disease]
- Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome [ORDO Disease]
- Early-onset progressive encephalopathy with migrant continuous myoclonus [ORDO Disease]
- Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome [ORDO Disease]
- Epilepsy with myoclonic absences [ORDO Disease]
- ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement [ORDO Disease]
- Idiopathic hemiconvulsion-hemiplegia syndrome [ORDO Disease]
- Infantile convulsions and choreoathetosis [ORDO Disease]
- Infantile epilepsy syndrome [ORDO Disease]
- Infantile epileptic-dyskinetic encephalopathy [ORDO Disease]
- Infantile spasms syndrome [ORDO Disease]
- Infantile spasms-broad thumbs syndrome [ORDO Disease]
- KCNQ2-related epileptic encephalopathy [ORDO Disease]
- Lennox-Gastaut syndrome [ORDO Disease]
- Lethal neonatal spasticity-epileptic encephalopathy syndrome [ORDO Disease]
- Moynahan syndrome [ORDO Disease]
- Myoclonic epilepsy in non-progressive encephalopathies [ORDO Disease]
- Myoclonic-astatic epilepsy [ORDO Disease]
- Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome [ORDO Disease]
- Neonatal epilepsy syndrome [ORDO Disease]
- Neonatal epileptic encephalopathy due to glutaminase deficiency [ORDO Disease]
- Non-specific early-onset epileptic encephalopathy [ORDO Disease]
- PRUNE1-related neurological syndrome [ORDO Disease]
- PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [ORDO Disease]
- PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation [ORDO Disease]
- Pachygyria-intellectual disability-epilepsy syndrome [ORDO Disease]
- Perioral myoclonia with absences [ORDO Disease]
- Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome [ORDO Disease]
- RNF13-related severe early-onset epileptic encephalopathy [ORDO Disease]
- Rare epilepsy [ORDO Disease]
- Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome [ORDO Disease]
- SYNGAP1-related developmental and epileptic encephalopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Epilepsy with myoclonic absences [ORDO Disease]
- Epileptic encephalopathies [ICD-11 Category]

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