raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:276267

OBSOLETE: Xeroderma pigmentosum complementation group G

inactive · referred to ORPHA:910Xeroderma pigmentosum

Synonyms: OBSOLETE: XPG

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 GOBSOLETE: XPG
frOBSOLETE : Xeroderma pigmentosum, groupe de complémentation GOBSOLETE : XPG
deOBSOLET: Xeroderma pigmentosum Komplementationsgruppe GOBSOLET: XPG
esOBSOLETO: Xeroderma pigmentoso grupo de complementación GOBSOLETO: XPG
itOBSOLETO: Xeroderma pigmentoso, gruppo di complementazione GOBSOLETO: XPG
nlOBSOLEET: Xeroderma pigmentosum complementatiegroep GOBSOLEET: XPG
ptOBSOLETO: Xeroderma pigmentoso, grupo de complementação G
plNIEAKTUALNE: Skóra pergaminowata barwnikowa grupa komplementacyjna GNIEAKTUALNE: XPG
csNEAKTUÁLNÍ: Xeroderma pigmentosum, typ GNEAKTUÁLNÍ: XPG · NEAKTUÁLNÍ: Xeroderma pigmentosum, komplementační skupina G
ukЗАСТАРІЛО: Ксеродермія пігментна, група комплементації GЗАСТАРІЛО: XPG
zh弃用:着色性干皮病G互补组XPG
trEski adı: Kseroderma pigmentozum komplemantasyon grubu GXPG
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