raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:240266

OBSOLETE: Systemic non-Langerhans cell histiocytosis

inactive · referred to ORPHA:157987Non-Langerhans cell histiocytosis

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Non-Langerhans cell histiocytosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Systemic non-Langerhans cell histiocytosis
frOBSOLETE : Histiocytose non-Langerhansienne systémique
deOBSOLET: Zell-Histiozytose, systemische (nicht Langerhans)
esOBSOLETO: Histiocitosis de células no-Langerhans sistémica
itOBSOLETO: Istiocitosi sistemica a cellule non Langerhans
nlOBSOLEET: Systemische niet-Langerhanscelhistiocytose
ptOBSOLETO: Histiocitose sistémica de células não-Langerhans
plNIEAKTUALNE: Ukladowa histiocytoza nie z komórek Langerhansa
csNEAKTUÁLNÍ: Systémová histiocytóza z non-Langerhansových buněk
ukЗАСТАРІЛО: Системний нелангергансівський гістіоцитоз
zh弃用:系统性非朗格汉斯细胞增生症
trEski adı: Sistemik Langerhans dışı hücreli histiyositoz
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