ORPHA:164823
Rare acquired aplastic anemia
- 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 | Rare acquired aplastic anemia | |
| fr | Aplasie médullaire acquise rare | |
| de | Aplastische Anämie, erworbene seltene | |
| es | Anemia aplásica adquirida rara | |
| it | Anemia aplastica acquisita rara | |
| nl | Zeldzame verworven aplastische anemie | |
| pt | Aplasia constitucional medular do adulto | |
| pl | Rzadka nabyta aplazja szpiku | |
| cs | Vzácné získané aplastické anémie | |
| uk | Рідкісна набута апластична анемія | |
| zh | 罕见获得性再生障碍性贫血 | |
| tr | Nadir edinsel aplastik anemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15610 | E | validated | |
| UMLS | C5680440 | 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:182040Rare aplastic anemia
rare hematological diseases; rare transplant-related disorders
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/164823
- This record as JSON: /data/d/164823.json