ORPHA:98363
Rare 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 hemolytic anemia | |
| fr | Anémie hémolytique rare | |
| de | Anämie, hämolytische | |
| es | Anemia hemolítica rara | |
| it | Anemia emolitica rara | |
| nl | Zeldzame hemolytische anemie | |
| pt | Anemia hemolítica | |
| pl | Rzadka niedokrwistość hemolityczna | |
| cs | Vzácné hemolytické anémie | |
| uk | Рідкісна гемолітична анемія | |
| zh | 罕见溶血性贫血 | |
| tr | Nadir hemolitik anemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681717 | 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:108997Rare anemia
rare hematological diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:178330OBSOLETE: Heinz body anemia referred to · inactive
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/98363
- This record as JSON: /data/d/98363.json