raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98287

Histiocytic and dendritic cell tumor

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enHistiocytic and dendritic cell tumor
frTumeur des histiocytes et des cellules dendritiques
deHistiozytischer und dendritischer Zell-Tumor
esTumor de células histiocíticas y dentríticas
itTumore delle cellule dendritiche e istiocitiche
nlHistiocytische en dendritische celtumor
ptTumor de células histiocíticas e dendríticas
plGuz z komórek histiocytarnych i dendrytycznych
csNádory z histiocytů a dendritických buněk
ukГістіоцитарна та дендритноклітинна пухлина
zh组织细胞和树突状细胞肿瘤
trHistiositik ve dendritik hücreli tümör
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0006247Evalidated
MONDO6247Evalidated
UMLSC1334030Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Annual incidence<1 / 1 000 0000.05 / 100 000EuropeValue and classValidatedRARECARE surveillance of rare cancers in Europe[OTHER]

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card