ORPHA:98844
Classic Hodgkin lymphoma, mixed cellularity type
- Type
- Histopathological subtype
- Group
- Subtype of disorder
- Age of onset
- Adult
- Status
- active
This disease is described under Classic Hodgkin lymphoma
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Classic Hodgkin lymphoma, mixed cellularity type | |
| fr | Lymphome de Hodgkin classique à cellularité mixte | |
| de | Klassisches Hodgkin-Lymphom, gemischtzelliges | |
| es | Linfoma de Hodgkin clásico de naturaleza celular mixta | |
| it | Linfoma di Hodgkin classico a cellularità mista | |
| nl | Klassiek Hodgkin-lymfoom, type gemengde cellulariteit | |
| pt | Linfoma de Hodgkin clássico, celularidade mista | |
| pl | Klasyczny chłoniak Hodgkina, typ mieszanokomórkowy | |
| cs | Klasický Hodgkinův lymfom, typu smíšené buněčnosti | |
| uk | Класична лімфома Ходжкіна, змішаний клітинний тип | |
| zh | 经典霍奇金淋巴瘤混合细胞型 | |
| tr | Klasik Hodgkin lenfoma, karma hücresel tip |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C81.2 | E | specific | validated |
| ICD-11 | 2B30.12 | E | specific | validated |
| MONDO | 0004633 | E | validated | |
| UMLS | C0152266 | E | validated | |
| MedDRA | 10020242 | 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:391Classic Hodgkin lymphoma
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.42 / 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/98844
- This record as JSON: /data/d/98844.json