ORPHA:268980

Isolated focal cortical dysplasia type Ib

Synonyms: FCD type Ib

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

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	0017097	E		validated
UMLS	C5679765	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:268961Isolated focal cortical dysplasia type I
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases

No children.

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.