ORPHA:171895
Myeloid hemopathy
- 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 | Myeloid hemopathy | |
| fr | Hémopathie myéloïde | |
| de | Myeloische Hämopathie | |
| es | Hemopatía mieloide | |
| it | Emopatia mieloide | |
| nl | Myeloïde hemopathie | |
| pt | Hemopatia mielóide | |
| pl | Hemopatia szpiku | |
| cs | Myeloidní hematologická onemocnění | Myeleoidní hemopatie |
| uk | Мієлоїдна гемопатія | |
| zh | 髓样血液病 | |
| tr | Miyeloid hemopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015756 | E | validated | |
| MONDO | 15756 | E | validated | |
| UMLS | C5680514 | 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 (2):
- ORPHA:506219Rare disorder potentially indicated for hematopoietic stem cell transplant
rare transplant-related disorders - ORPHA:68347Tumor of hematopoietic and lymphoid tissues
rare hematological diseases; rare neoplastic diseases
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/171895
- This record as JSON: /data/d/171895.json