ORPHA:98375
Autoimmune hemolytic anemia
Synonyms: AHA · AIHA
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Multigenic/multifactorial
- Age of onset
- All ages
- Status
- active
A rare, autoimmune disorder in which various types of auto-antibodies are directed against red blood cells causing their survival to be shortened and resulting in hemolytic anemia.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Autoimmune hemolytic anemia | AHA · AIHA |
| fr | Anémie hémolytique auto-immune | AHA · AHAI · AIHA |
| de | Anämie, autoimmun-hämolytische | |
| es | Anemia hemolítica autoinmune | AHA · AHAI |
| it | Anemia emolitica autoimmune | = en |
| nl | Auto-immune hemolytische anemie | = en |
| pt | Anemia hemolítica autoimune | |
| pl | Autoimmunologiczna niedokrwistość hemolityczna | = en |
| cs | Autoimunitní hemolytická anémie | = en |
| uk | Аутоімунна гемолітична анемія | АНА · AIHA |
| zh | 自身免疫性溶血性贫血 | 自免溶贫 |
| tr | Otoimmün hemolitik anemi | = en |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 3A20 | E | specific | validated |
| MONDO | 0020108 | E | validated | |
| MeSH | D000744 | E | validated | |
| UMLS | C0002880 | E | validated | |
| GARD | 5870 | E | validated | |
| MedDRA | 10002046 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:182047Rare acquired hemolytic anemia
rare hematological diseases
Children (6):
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
4 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 2.02 / 100 000 | Europe | Value and class | Validated | [EXPERT]_ORPHANET |
| Annual incidence | 1-9 / 100 000 | 2.02 / 100 000 | United States | Value and class | Validated | [EXPERT]_ORPHANET |
| Point prevalence | 1-5 / 10 000 | 11 / 100 000 | Denmark | Value and class | Validated | 20066507[PMID] |
| Point prevalence | 1-9 / 100 000 | — | Europe | Class only | Not yet validated | ORPHANET |
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98375
- This record as JSON: /data/d/98375.json