Epilepsy due to genetic disease
genetische aandoening
lichte malformatie van corticale ontwikkeling
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lichte malformatie van corticale ontwikkeling met oligodendrogliale hyperplasie en epilepsie (aandoening)
lichte malformatie van corticale ontwikkeling met oligodendrogliale hyperplasie en epilepsie
MOGHE
mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy
lichte afwijking van hersenschorsontwikkeling met oligodendrogliale hyperplasie en epilepsie
mMCD met oligodendrogliale hyperplasie en epilepsie
lichte misvorming van corticale ontwikkeling met oligodendrogliale hyperplasie en epilepsie
lichte MCD met oligodendrogliale hyperplasie en epilepsie
Mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy
MOGHE - mild malformation of cortical development, oligodendroglial hyperplasia, epilepsy
Id1402140007
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van cortex cerebri
Pathological processproces van pathologische ontwikkeling
Associated morphologyhyperplasie
Finding siteoligodendrocyt
SNOMED CT to ICD-10 extended map
TargetQ04.8
RuleTRUE
AdviceALWAYS Q04.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetG40.1
RuleTRUE
AdviceALWAYS G40.1 | MAPPED FOLLOWING WHO GUIDANCE
CorrelationSNOMED CT source code to target map code correlation not specified