ORPHA:268961

Isolated focal cortical dysplasia type I

Synonyms: FCD type I

Orphadata ships no English definition for this code.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Isolated focal cortical dysplasia type I	FCD type I
fr	Dysplasie corticale focale isolée type I	= en
de	Kortikale Dysplasie, fokale isolierte, Typ I	FCD Typ I
es	Displasia cortical focal aislada tipo I	FCD tipo I
it	Displasia corticale focale isolata tipo I	FCD tipo I
nl	Geïsoleerde focale corticale dysplasie type I	= en
pt	Displasia cortical focal isolada tipo I	FCD tipo I
pl	Izolowana dysplazja korowa mózgu typu I	FCD typu I
cs	Izolovaná fokální kortikální dysplázie, typ I	FCD typ I
uk	Ізольована фокальна кортикальна дисплазія, тип I	FCD тип I
zh	孤立性局灶性脑皮质发育不良I型	FCD I型
tr	İzole fokal kortikal displazi tip I	FCD tip I

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	Q04.8	NTBT	attributed	validated
ICD-11	LA05.51	NTBT	index	validated
MONDO	0017095	E		validated
UMLS	C5679772	E		validated

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

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

ORPHA:65683Isolated focal cortical dysplasia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases

Children (3):

0 direct

Orphanet records no gene directly on this code.

1 record

Type	Class	Value	Area	Qualification	Validation	Source
Point prevalence	Unknown	—	Worldwide	Class only	Not yet validated	ORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

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