ORPHA:178548
Indolent primary cutaneous T-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| Lang | Name | Synonyms |
|---|---|---|
| en | Indolent primary cutaneous T-cell lymphoma | |
| fr | Lymphome T cutané primitif d'évolution indolente | |
| de | Primär kutanes T-Zell-Lymphom, indolentes | |
| es | Linfoma cutáneo primario de células T indolente | |
| it | Linfoma cutaneo primitivo indolente a cellule T | |
| nl | Indolent primair cutaan T-cellymfoom | |
| pt | Linfoma cutâneo de células T, indolente | |
| pl | Pierwotny skórny chłoniak T-komórkowy o powolnym przebiegu | |
| cs | Primární kožní T-buněčný lymfom s indolentním průběhem | Primární kožní indolentní T-buněčný lymfom |
| uk | Первинна первинна шкірна Т-клітинна лімфома в стані спокою | |
| zh | 惰性原发性皮肤T细胞淋巴瘤 | |
| tr | Ağrısız primer kutanöz T hücreli lenfoma |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015816 | E | validated | |
| MONDO | 15816 | E | validated | |
| UMLS | C5680498 | 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:171901Primary cutaneous T-cell lymphoma
rare skin diseases; rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/178548
- This record as JSON: /data/d/178548.json