ORPHA:182047
Rare acquired hemolytic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare acquired hemolytic anemia | |
| fr | Anémie hémolytique acquise rare | |
| de | Hämolytische Anämie, erworbene, seltene | |
| es | Anemia hemolítica adquirida rara | |
| it | Anemia emolitica acquisita rara | |
| nl | Zeldzame verworven hemolytische anemie | |
| pt | Anemia hemolítica adquirida rara | |
| pl | Rzadka nabyta niedokrwistość hemolityczna | |
| cs | Vzácné získané hemolytické anémie | |
| uk | Рідкісна набута гемолітична анемія | |
| zh | 罕见获得性溶血性贫血 | |
| tr | Nadir edinsel hemolitik anemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15911 | E | validated | |
| UMLS | C5680604 | 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:98363Rare hemolytic anemia
rare hematological 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/182047
- This record as JSON: /data/d/182047.json