ORPHA:547
Non-Hodgkin lymphoma
Synonyms: NHL
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Adolescent, Adult, Childhood, Elderly, Infancy
- Status
- active
A heterogeneous group of malignant tumors of the lymphoid system.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-Hodgkin lymphoma | NHL |
| fr | Lymphome malin non-hodgkinien | LMNH · LNH |
| de | Non-Hodgkin-Lymphom | = en |
| es | Linfoma no Hodgkin | LNH |
| it | Linfoma non-Hodgkin | LNH |
| nl | Non-Hodgkin-lymfoom | = en |
| pt | Linfoma maligno não-Hodgkin | = en |
| pl | Chłoniak nieziarniczy | = en |
| cs | Non-Hodgkinův lymfom | = en |
| uk | Неходжкінські лімфоми | = en |
| zh | 非霍奇金淋巴瘤 | = en |
| tr | Hodgkin dışı lenfoma | = en |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 605027 | BTNT | validated | |
| MONDO | 0018908 | E | validated | |
| MONDO | 18908 | E | validated | |
| MeSH | D008228 | E | validated | |
| UMLS | C0024305 | E | validated | |
| MedDRA | 10029547 | 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:223735Lymphoma
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:329998OBSOLETE: Lymphomatous meningitis referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-5 / 10 000 | — | Europe | Class only | Not yet validated | 22835603[PMID] |
| Annual incidence | 1-5 / 10 000 | 11.6 / 100 000 | Europe | Value and class | Validated | RARECARE 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.
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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/547
- This record as JSON: /data/d/547.json