Autosomal recessive hereditary disorder	Familial disease	Hereditary disorder of nervous system	Myoclonic seizure
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Familial infantile myoclonic epilepsy (disorder)
	Familial infantile myoclonic epilepsy
	Familial infantile myoclonus epilepsy FIME - familial infantile myoclonic epilepsy
	A rare genetic infantile epilepsy syndrome disease with characteristics of neonatal to infancy onset myoclonic focal seizures occurring in various members of a family, associated in some with mild dysarthria, ataxia and borderline-to-moderate intellectual disability.
	familiaire infantiele myoklonische epilepsie
	familiaire infantiele myoclonusepilepsie

Id	784342008
Status	Primitive

Finding site	Cerebrum
Occurrence	Infancy

Interprets

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G40.3
Rule	TRUE
Advice	ALWAYS G40.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified