ORPHA:178563
Primary cutaneous B-cell 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary cutaneous B-cell lymphoma | |
| fr | Lymphome B cutané primitif | |
| de | Primär kutanes B-Zell-Lymphom | |
| es | Linfoma cutáneo primario de células B | |
| it | Linfoma cutaneo primitivo a cellule B | |
| nl | Primair cutaan B-cellymfoom | |
| pt | Linfoma cutâneo de células B | |
| pl | Pierwotny chłoniak skóry B-komórkowy | |
| cs | Primární kožní B-buněčný lymfom | |
| uk | Первинна шкірна В-клітинна лімфома | |
| zh | 原发性皮肤B细胞淋巴瘤 | |
| tr | Primer kutanöz B hücreli lenfoma |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015820 | E | validated | |
| MONDO | 15820 | E | validated | |
| UMLS | C1274310 | E | validated | |
| MedDRA | 10085518 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:542Primary cutaneous lymphoma
rare skin diseases; rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/178563
- This record as JSON: /data/d/178563.json