ORPHA:97295

Furlong syndrome

Synonyms: Marfanoid habitus-craniosynostosis syndrome

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Loeys-Dietz syndrome

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Furlong syndrome	Marfanoid habitus-craniosynostosis syndrome
fr	Syndrome de Furlong	Craniosynostose marfanoïde
de	Furlong-Syndrom	Marfanoider Habítus-Kraniosynostose-Syndrom
es	Síndrome de Furlong	Constitución marfanoide-síndrome de craneosinostosis · Hábito marfanoide-síndrome de craneosinostosis
it	Sindrome di Furlong	Craniosinostosi marfanoide
nl	Syndroom van Furlong	Marfanoïde habitus - craniosynostose-syndroom
pt	Síndrome Furlong	Síndrome habitus marfanóide-craniosinostose
pl	Zespół Furlonga	Zespół sylwetki marfanoidalalnej z kraniosynostozą
cs	Syndrom Furlongové	Syndrom zahrnující marfanoidní habitus a kraniosynostózu
uk	Синдром Фурлонга	Синдром марфаноїдного габітусу-краніосиностозу
zh	Furlong综合征	马方综合征样体型-颅缝早闭综合征
tr	Furlong sendromu	Marfanoid habitus-kraniyosinostoz sendromu

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MeSH	C538192	E		validated
UMLS	C2931764	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.