ORPHA:98846
Classic Hodgkin lymphoma, lymphocyte-depleted type
- Type
- Histopathological subtype
- Group
- Subtype of disorder
- Age of onset
- Adult
- Status
- active
This disease is described under Classic Hodgkin lymphoma
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Classic Hodgkin lymphoma, lymphocyte-depleted type | |
| fr | Lymphome de Hodgkin classique pauvre en lymphocytes | |
| de | Klassisches Hodgkin-Lymphom, lymphozytenarmes | |
| es | Linfoma de Hodgkin clásico tipo depleción linfocítica | |
| it | Linfoma di Hodgkin classico, povero di linfociti | |
| nl | Klassiek Hodgkin-lymfoom, lymfocytarm type | |
| pt | Linfoma de Hodgkin clássico, pobre em linfócitos | |
| pl | Klasyczny chłoniak Hodgkina, typ ubogolimfocytarny | |
| cs | Klasický Hodgkinův lymfom, typ lymfocytární deplece | |
| uk | Класична лімфома Ходжкіна, лімфоцитарна недостатність | |
| zh | 经典霍奇金淋巴瘤淋巴细胞消减型 | |
| tr | Klasik Hodgkin lenfoma, lenfositten yoksun tip |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C81.3 | E | specific | validated |
| ICD-11 | 2B30.13 | E | specific | validated |
| MONDO | 0004620 | E | validated | |
| UMLS | C0152267 | E | validated | |
| MedDRA | 10020219 | E | validated |
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 (1):
- ORPHA:391Classic Hodgkin lymphoma
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | 0.04 / 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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98846
- This record as JSON: /data/d/98846.json