raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:276258

OBSOLETE: Xeroderma pigmentosum complementation group D

inactive · referred to ORPHA:910Xeroderma pigmentosum

Synonyms: OBSOLETE: XPD

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Xeroderma pigmentosum

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Xeroderma pigmentosum complementation group DOBSOLETE: XPD
frOBSOLETE : Xeroderma pigmentosum, groupe de complémentation DOBSOLETE : XPD
deOBSOLET: Xeroderma pigmentosum Komplementationsgruppe DOBSOLET: XPD
esOBSOLETO: Xeroderma pigmentoso grupo de complementación DOBSOLETO: XPD
itOBSOLETO: Xeroderma pigmentoso, gruppo di complementazione DOBSOLETO: XPD
nlOBSOLEET: Xeroderma pigmentosum complementatiegroep DOBSOLEET: XPD
ptOBSOLETO: Xeroderma pigmentoso, grupo de complementação D
plNIEAKTUALNE: Skóra pergaminowata barwnikowa grupa komplementacyjna DNIEAKTUALNE: XPD
csNEAKTUÁLNÍ: Xeroderma pigmentosum, typ DNEAKTUÁLNÍ: XPD · NEAKTUÁLNÍ: Xeroderma pigmentosum, komplementační skupina D
ukЗАСТАРІЛО: Ксеродермія пігментна, група комплементації DЗАСТАРІЛО: XPD
zh弃用:着色性干皮病D互补组XPD
trEski adı: Kseroderma pigmentozum komplemantasyon grubu DXPD
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