ORPHA:98275
Myelodysplastic/myeloproliferative disease
- Type
- Clinical group
- 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 | Myelodysplastic/myeloproliferative disease | |
| fr | Maladie myélodysplasique/myéloproliférative | |
| de | Myeloproliferative/Myelodysplastische Krankheit | |
| es | Enfermedad mielodisplásica o mieloproliferativa | |
| it | Malattia mieloproliferativa o mielodisplastica | |
| nl | Myelodysplastische/myeloproliferatieve aandoening | |
| pt | Doença mielodisplástica ou mieloproliferativa | |
| pl | Choroba mielodysplastyczna/mieloproliferacyjna | |
| cs | Myelodysplastická/myeloproliferativní onemocnění | |
| uk | Мієло диспластичне/мієлопроліферативне захворювання | |
| zh | 骨髓增生异常/骨髓增殖性疾病 | |
| tr | Miyelodisplastik / miyeloproliferatif hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020077 | E | validated | |
| MeSH | D054437 | E | validated | |
| UMLS | C1301355 | E | validated | |
| GARD | 9351 | 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:171895Myeloid hemopathy
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
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 | 1-9 / 1 000 000 | 0.29 / 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/98275
- This record as JSON: /data/d/98275.json