8A61.2Y Other specified genetic epileptic syndromes with childhood onset
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Other specified genetic epileptic syndromes with childhood onset
- Generalised epilepsy - paroxysmal dyskinesia
- Generalised epilepsy with febrile seizures plus
- Benign occipital epilepsy
- Early onset benign occipital epilepsy, Panayiotopoulos type
- Panayiotopoulos syndrome
- Late onset childhood occipital epilepsy, Gastaut type
- Idiopathic childhood occipital epilepsy of Gastaut
- Myoclonic epilepsy in early childhood
- Epilepsy with myoclonic-atonic seizures
- Perioral myoclonia with absences
- Jeavons syndrome
- Cryptogenic late-onset epileptic spasms
- Rolandic epilepsy-speech dyspraxia syndrome
- Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
- Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
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