ORPHA:98291
Lymphoproliferative disease associated with primary immune disease
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Childhood
- 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 | Lymphoproliferative disease associated with primary immune disease | |
| fr | Syndrome lymphoprolifératif associé à un déficit immunitaire primaire | |
| de | Lymphoproliferative Krankheit mit assoziiertem primären Imundefekt | |
| es | Enfermedad linfoproliferativa asociada con la inmunodeficiencia primaria | |
| it | Malattia linfoproliferativa associata a malattia immune primaria | |
| nl | Lymfoproliferatieve ziekte geassocieerd met primaire immuunziekte | |
| pt | Doença linfoproliferativa associada a doença imune primária | |
| pl | Choroba limfoproliferacyjna z towarzyszącym pierwotnym niedoborem odporności | |
| cs | Lymfoproliferativní onemocnění spojená s primární poruchou imunity | |
| uk | Лімфопроліферативне захворювання, повязане з первинним імунним захворюванням | |
| zh | 原发性免疫疾病相关淋巴增殖性疾病 | |
| tr | Primer bağışıklık hastalığı -ilişkili lenfoproliferatif hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681532 | 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:98290Immunodeficiency-associated lymphoproliferative disease
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
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/98291
- This record as JSON: /data/d/98291.json