raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1956

OBSOLETE: Erythromelalgia

inactive · referred to ORPHA:90026Primary erythromelalgia

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Erythromelalgia
frOBSOLETE : Erythromélalgie
deOBSOLET: Erythromelalgie
esOBSOLETO: Eritromelalgia
itOBSOLETO: Eritromelalgia
nlOBSOLEET: Erytromelalgie
ptOBSOLETO: Eritromelalgia
plNIEAKTUALNE: Erytromelalgia
csNEAKTUÁLNÍ: Erytromelalgie
ukЗАСТАРІЛО: Еритромелалгія
zh弃用:红斑性肢痛症
trEski adı: Eritromelalji
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