ORPHA:98843
Classic Hodgkin lymphoma, nodular sclerosis 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, nodular sclerosis type | |
| fr | Lymphome de Hodgkin classique type sclérosant nodulaire | |
| de | Klassisches Hodgkin-Lymphom, nodulär-sklerosierendes | |
| es | Linfoma de Hodgkin clásico con esclerosis nodular | |
| it | Linfoma di Hodgkin classico, tipo nodulare sclerosante | |
| nl | Klassiek Hodgkin-lymfoom, type nodulaire sclerose | |
| pt | Linfoma de Hodgkin clássico, esclerose nodular | |
| pl | Klasyczny chłoniak Hodgkina, typ ze stwardnieniem guzkowym | |
| cs | Klasický Hodgkinův lymfom, typ nodulární sklerózy | |
| uk | Класична лімфома Ходжкіна, тип вузликового склерозу | |
| zh | 经典霍奇金淋巴瘤结节硬化型 | |
| tr | Klasik Hodgkin lenfoma, nodüler skleroz tipi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C81.1 | E | specific | validated |
| ICD-11 | 2B30.10 | E | specific | validated |
| MONDO | 0020327 | E | validated | |
| MONDO | 4665 | E | validated | |
| UMLS | C0152268 | E | validated | |
| MedDRA | 10020244 | 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
1 direct| Gene | Association | Status | HGNC | Ensembl | OMIM | Locus | Name | Source of validation |
|---|---|---|---|---|---|---|---|---|
| KLHDC8B | Candidate gene tested in | Not yet assessed | HGNC:28557 | ENSG00000185909 | 613169 | 3p21.31 | kelch domain containing 8B | 19706467[PMID] |
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 1.28 / 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/98843
- This record as JSON: /data/d/98843.json