raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:374

Goldenhar syndrome

inactive · moved to ORPHA:141132Craniofacial microsomia

Synonyms: Facioauriculovertebral sequence

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Oculo-auriculo-vertebral spectrum

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enGoldenhar syndromeFacioauriculovertebral sequence
frSyndrome de GoldenharSéquence facioauriculovertébrale
deGoldenhar-Syndrom
esSíndrome de GoldenharSecuencia facio-aurículo-vertebral
itSindrome di GoldenharDisplasia OAV · Displasia facio-auricolo-vertebrale · Displasia oculo-auricolo-vertebrale · Microsomia craniofacciale · OAVS · Sindrome oculo-auricolo-vertebrale · Spettro allargato della microsomia emifacciale · Spettro oculo-auricolo-vertebrale
nlSyndroom van GoldenharFacioauriculovertebrale sequentie
ptSíndrome GoldenharDisplasia óculo-auriculo-vertebral · Microssomia hemifacial
plZespół GoldenharaDysplazja OAV · Dysplazja oczno-uszno-kręgowa/kręgosłupowa · Dysplazja twarzowo-uszno-kręgowa/kręgosłupowa · OAVS · Rozszerzone spektrum mikrosomii połowy twarzy · Spektrum oczno-uszno-kręgowe/kręgosłupowe · Zespół oczno-uszno-kręgowy/kręgosłupowy
csGoldenharův syndromFacioaurikulovertebrální sekvence · OAV · OAVS · Okuloaurikulovertebrální dysplázie · Okuloaurikulovertebrální syndrom
ukСиндром ГольденхараФаціоаурикуловертебральна послідовність
zhGoldenhar综合征面-耳-脊椎序列征
trGoldenhar sendromuFasiyoaurikulovertebral dizi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MeSHD006053Evalidated

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

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card