raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:141330

OBSOLETE: Orofaciodigital syndrome type 13

inactive · referred to ORPHA:140997Orofaciodigital syndrome

Synonyms: OBSOLETE: Degner syndrome · OBSOLETE: OFD13 · OBSOLETE: Oral-facial-digital syndrome type 13

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Orofaciodigital syndrome type 13OBSOLETE: Degner syndrome · OBSOLETE: OFD13 · OBSOLETE: Oral-facial-digital syndrome type 13
frOBSOLETE : Syndrome oro-facio-digital type 13OBSOLETE : OFD13 · OBSOLETE : Syndrome de Degner
deOBSOLET: Oro-fazio-digitales Syndrom Typ 13OBSOLET: Degner-Syndrom · OBSOLET: OFD13 · OBSOLET: Oral-fazial-digitales Syndrom Typ 13
esOBSOLETO: Síndrome orofaciodigital tipo 13OBSOLETO: OFD13 · OBSOLETO: Síndrome de Degner · OBSOLETO: Síndrome oro-facio-digital tipo 13
itOBSOLETO: Sindrome oro-facio-digitale, tipo 13OBSOLETE: Sindrome oro-facio-digitale, tipo 13 · OBSOLETO: OFD13 · OBSOLETO: Sindrome di Degner · OBSOLETO: Sindrome oro-facio-digitale tipo 13 · OBSOLETE: OFD13
nlOBSOLEET: Orofaciodigitaal syndroom type 13OBSOLEET: OFD13 · OBSOLEET: Oraal-faciaal-digitaal syndroom type 13 · OBSOLEET: Syndroom van Degner
ptOBSOLETO: Síndrome orofaciodigital tipo 13
plNIEAKTUALNE: Zespół ustno-twarzowo-palcowy typu 13NIEAKTUALNE: OFD13
csNEAKTUÁLNÍ: Orofaciodigitální syndrom, typ 13NEAKTUÁLNÍ: OFD13
ukЗАСТАРІЛО: Орофаціодигітальний синдром, тип 13ЗАСТАРІЛО: Синдром Дегнера · ЗАСТАРІЛО: OFD13 · ЗАСТАРІЛО: Орально-лицево-пальцевий синдром, тип 13
zh口面指综合征13型口-面-指综合征13型
trOrofasiyodijital sendrom tip 13OFD13 · Degner sendromu · Oral-fasiyal-dijital sendromu tip 13

Definition in:

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