raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98844

Classic Hodgkin lymphoma, mixed cellularity type

Type
Histopathological subtype
Group
Subtype of disorder
Age of onset
Adult
Status
active

This disease is described under Classic Hodgkin lymphoma

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enClassic Hodgkin lymphoma, mixed cellularity type
frLymphome de Hodgkin classique à cellularité mixte
deKlassisches Hodgkin-Lymphom, gemischtzelliges
esLinfoma de Hodgkin clásico de naturaleza celular mixta
itLinfoma di Hodgkin classico a cellularità mista
nlKlassiek Hodgkin-lymfoom, type gemengde cellulariteit
ptLinfoma de Hodgkin clássico, celularidade mista
plKlasyczny chłoniak Hodgkina, typ mieszanokomórkowy
csKlasický Hodgkinův lymfom, typu smíšené buněčnosti
ukКласична лімфома Ходжкіна, змішаний клітинний тип
zh经典霍奇金淋巴瘤混合细胞型
trKlasik Hodgkin lenfoma, karma hücresel tip
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C81.2Especificvalidated
ICD-112B30.12Especificvalidated
MONDO0004633Evalidated
UMLSC0152266Evalidated
MedDRA10020242Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Annual incidence1-9 / 1 000 0000.42 / 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