ORPHA:98290
Immunodeficiency-associated lymphoproliferative disease
- Type
- Category
- 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 | Immunodeficiency-associated lymphoproliferative disease | |
| fr | Déficit immunitaire associé à un syndrome lymphoprolifératif | Immunodéficience associée à un syndrome lymphoprolifératif |
| de | Immundefekt mit assoziierter lymphoproliferativer Krankheit | |
| es | Inmunodeficiencia asociada a enfermedad linfoproliferativa | |
| it | Malattia linfoproliferativa correlata a immunodeficienza | |
| nl | Immuundeficiëntiegeassocieerde lymfoproliferatieve ziekte | |
| pt | Doença linfoproliferativa associada a imunodeficiência | |
| pl | Niedobór odporności towarzyszący chorobie limfoproliferacyjnej | |
| cs | Lymfoproliferativní onemocnění spojená s imunodeficiencí | |
| uk | Імунодефіцит-асоційоване лімфопроліферативне захворювання | |
| zh | 免疫缺陷相关淋巴增殖性疾病 | |
| tr | İmmün yetmezliğe bağlı lenfoproliferatif hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 2B32 | E | specific | validated |
| MONDO | 0020083 | E | validated | |
| UMLS | C5681530 | 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:171898Lymphoid hemopathy
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
Children (4):
- ORPHA:98291Lymphoproliferative disease associated with primary immune disease
- ORPHA:86904Methotrexate-associated lymphoproliferative disorders
- ORPHA:70568Post-transplant lymphoproliferative disease
- ORPHA:675628TLR8-related inflammation-severe neutropenia-bone marrow failure-lymphoproliferation syndrome
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/98290
- This record as JSON: /data/d/98290.json