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familiaire mesiale temporalekwabepilepsie met epileptische aanvallen geprovoceerd door koorts (aandoening)
familiaire mesiale temporalekwabepilepsie met epileptische aanvallen geprovoceerd door koorts
familiaire mesiale temporale epilepsie met koortsconvulsies
familiaire mesiale temporale epilepsie met koortsstuipen
Familial mesial temporal lobe epilepsy with febrile seizures
A rare genetic familial partial epilepsy disease with characteristics of simple partial seizures, complex partial seizures and/or secondarily generalized seizures, originating from the inner aspect of the temporal lobe, associated with an antecedent history of febrile seizures, occurring in various members of a family. Hippocampal abnormalities (for example hippocampal sclerosis) may also be associated. There is evidence the disease is caused by homozygous mutation in the CPA6 gene on chromosome 8q13.
Id784372002
StatusPrimitive
Associated withkoorts
referentieset met complexe 'mapping' naar ICD-10
TargetG40.2
RuleTRUE
AdviceALWAYS G40.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified