raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98846

Classic Hodgkin lymphoma, lymphocyte-depleted 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, lymphocyte-depleted type
frLymphome de Hodgkin classique pauvre en lymphocytes
deKlassisches Hodgkin-Lymphom, lymphozytenarmes
esLinfoma de Hodgkin clásico tipo depleción linfocítica
itLinfoma di Hodgkin classico, povero di linfociti
nlKlassiek Hodgkin-lymfoom, lymfocytarm type
ptLinfoma de Hodgkin clássico, pobre em linfócitos
plKlasyczny chłoniak Hodgkina, typ ubogolimfocytarny
csKlasický Hodgkinův lymfom, typ lymfocytární deplece
ukКласична лімфома Ходжкіна, лімфоцитарна недостатність
zh经典霍奇金淋巴瘤淋巴细胞消减型
trKlasik Hodgkin lenfoma, lenfositten yoksun tip
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C81.3Especificvalidated
ICD-112B30.13Especificvalidated
MONDO0004620Evalidated
UMLSC0152267Evalidated
MedDRA10020219Evalidated

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 incidence<1 / 1 000 0000.04 / 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