raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:369902

OBSOLETE: DDX59-related orofaciodigital syndrome

inactive · referred to ORPHA:2919Orofaciodigital syndrome type 5

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Orofaciodigital syndrome type 5

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: DDX59-related orofaciodigital syndrome
frOBSOLETE : Syndrome oro-facio-digital lié à DDX59
deOBSOLET: Oro-fazio-digitales Syndrom Typ 14OBSOLET: OFD14
esOBSOLETO: Síndrome orofaciodigital tipo 14OBSOLETO: OFD14
itOBSOLETO: Sindrome orofaciodigitale, tipo 14OBSOLETO: OFD14 · OBSOLETO: Sindrome oro-facio-digitale, tipo 14
nlOBSOLEET: DDX59-gerelateerd orofaciodigitaal syndroomOBSOLEET: OFD14 · OBSOLEET: Orofaciodigitaal syndroom type 14
ptOBSOLETO: Síndrome oro-facio-digital DDX59-relacionadoOBSOLETO: OFD14 · OBSOLETO: Síndrome orofaciodigital tipo 14
plNIEAKTUALNE: Zespól ustno-twarzowo-palcowy typu 14NIEAKTUALNE: OFD14
csNEAKTUÁLNÍ: DDX59-vázaný orofaciodigitální syndrom
ukЗАСТАРІЛО: Орофаціодігітальний синдром, повязаний з DDX59
zh弃用:DDX59基因相关口-面-指综合征
trEski adı: DDX59-ilişkili orofasiyodijital sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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