raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:279911

Primary organ-specific lymphoma

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
enPrimary organ-specific lymphoma
frLymphome primaire spécifique d'organe
deOrgan-spezifisches Lymphom, primäres
esLinfoma órgano-específico primario
itLinfoma organo-specifico primitivo
nlPrimair orgaanspecifiek lymfoom
ptLinfoma órgão-específico primário
plPierwotny chłoniak specyficzny narządowo
csPrimární orgánově specifický lymfom
ukПервинна органоспецифічна лімфома
zh原发性器官特异性淋巴瘤
trPrimer organa özgü lenfoma
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0017207Evalidated
MONDO17207Evalidated
UMLSC5680788Evalidated

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):

  • ORPHA:223735Lymphoma
    rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders

Children (8):

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