ORPHA:168943
Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2 | |
| fr | Tumeur myéloïde/lymphoïde avec éosinophiles associée à une anomalie de PDGFRA, PDGFRB, FGFR1 ou JAK2 | |
| de | Myeloische/lymphatische Neoplasie mit assoziierter Eosinophilie und Veränderungen von PDGFRA, PDGFRB oder JAK2 | |
| es | Neoplasias mieloides/linfoides asociadas a eosinofilia y anomalías en los genes PDGFRA, PDGFRB, FGFR1 o JAK2 | |
| it | Neoplasie mieloidi associate ad eosinofilia e anomalie di PDGFRA, PDGFRB o FGRF1 | |
| nl | Myeloïde/lymfoïde neoplasmata geassocieerd met eosinofilie en afwijking van PDGFRA, PDGFRB, FGFR1 of JAK2 | |
| pt | Neoplasias mielóides/linfóides associadas a eosinofilia e anomalia de PDGFRA, PDGFRB, FGRF1 ou JAK2 | |
| pl | Nowotwory szpiku związane z eozynofilią i nieprawidłowościami PDGFRA, PDGFRB lub FGFR1 | |
| cs | Myeloidní neoplázie spojená s eozinofilií a abnormalitou PDGFRA, PDGFRB nebo FGFR1 | |
| uk | Мієлоїдні/лімфоїдні новоутворення, повязані з еозинофілією та аномалією PDGFRA, PDGFRB, FGFR1 або JAK2 | |
| zh | 嗜酸性粒细胞增多及PDGFRA、PDGFRB或FGFR1异常相关髓系/淋巴系肿瘤 | |
| tr | Eozinofili ilişkili miyeloid/lenfoid neoplazmalar ve PDGFRA, PDGFRB veya FGFR1 anormalliği |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015688 | E | validated | |
| MONDO | 15688 | E | validated | |
| UMLS | C5680457 | 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:171895Myeloid hemopathy
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
Children (4):
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/168943
- This record as JSON: /data/d/168943.json