ORPHA:352582

Familial infantile myoclonic epilepsy

Synonyms: FIME · Familial infantile myoclonus epilepsy

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Myoclonic epilepsy of infancy

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Familial infantile myoclonic epilepsy	FIME · Familial infantile myoclonus epilepsy
fr	Epilepsie myoclonique infantile familiale	FIME
de	Myoklonusepilepsie, infantile familiäre	FIME
es	Epilepsia mioclónica familiar del lactante	FIME
it	Epilessia mioclonica infantile familiare	FIME
nl	Familiale infantiele myoclonische epilepsie	FIME
pt	Epilepsia mioclónica familiar da infância	FIME
pl	Rodzinna dziecięca padaczka miokloniczna	FIME
cs	Familiární infantilní myoklonická epilepsie	FIME · Familiární kojenecká myoklonická epilepsie
uk	Сімейна інфантильна міоклонічна епілепсія	Сімейна інфантильна міоклонусна епілепсія · FIME
zh	家族性婴儿肌阵挛性癫痫	家族性婴儿肌阵挛癫痫
tr	Ailesel infantil miyoklonik epilepsi	FIME · Ailesel infantil miyoklonus epilepsisi

Definition in:

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	0011506	E		validated
UMLS	C0917800	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.