raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:178557

Indolent primary cutaneous B-cell lymphoma

Type
Clinical group
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
enIndolent primary cutaneous B-cell lymphoma
frLymphome B cutané primitif d'évolution indolente
dePrimär kutanes B-Zell-Lymphom, indolentes
esLinfoma cutáneo primario de células B indolente
itLinfoma cutaneo primitivo indolente a cellule B
nlIndolent primair cutaan B-cellymfoom
ptLinfoma cutâneo de células B, indolente
plPierwotny skórny chłoniak B-komórkowy o powolnym przebiegu
csPrimární kožní B-buněčný lymfom s indolentním průběhemPrimární kožní indolentní B-buněčný lymfom
ukПервинна первинна шкірна В-клітинна лімфома в стані спокою
zh惰性原发性皮肤B细胞淋巴瘤
trAğrısız primer kutanöz B hücreli lenfoma
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0015819Evalidated
MONDO15819Evalidated
UMLSC5680499Evalidated

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 (2):

Children (2):

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