Autoimmune hemolytic anemia, cold type
Synonyms: cAHA · cAIHA · Cold AIHA
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Multigenic/multifactorial
- Age of onset
- All ages
- Status
- active
Cold autoimmune hemolytic anemia comprises two types of autoimmune hemolytic anemia (AIHA) defined by the presence of cold autoantibodies (autoantibodies which are active at temperatures below 30 °C): cold agglutinin disease (CAD), which is the more common, and paroxysmal cold hemoglobinuria (PCH).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Autoimmune hemolytic anemia, cold type | cAHA · cAIHA · Cold AIHA |
| fr | Anémie hémolytique auto-immune à auto-anticorps froids | AIHA froid · cAHA · cAIHA |
| de | Anämie, autoimmun-hämolytische, Kälte-Typ | |
| es | Anemia hemolítica autoinmune con autoanticuerpos fríos | AHAI con autoanticuerpos fríos · AIHA con autoanticuerpos fríos |
| it | Anemia emolitica autoimmune da autoanticorpi freddi | AIHA fredda · cAHA · cAIHA |
| nl | Auto-immune hemolytische anemie, koude-type | Auto-immune hemolytische anemie met koude auto-antilichamen · Koude AIHA · cAHA · cAIHA |
| pt | Anemia hemolítica autoimune, do frio | |
| pl | Autoimmunologiczna niedokrwistość hemolityczna, typu zimnego | = en |
| cs | Chladová AIHA | Autoimunitní hemolytická anémie, chladový typ · cAHA · cAIHA |
| uk | Аутоімунна гемолітична анемія, холодний тип | cAHA · cAIHA · Холодний AIHA |
| zh | 自身免疫性溶血性贫血冷型 | AIHA冷型 |
| tr | Otoimmün hemolitik anemi, soğuk tip | cAHA · cAIHA · Soğuk AIHA |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 3A20.1 | E | specific | validated |
| MONDO | 0016450 | E | validated | |
| MONDO | 16450 | E | validated | |
| UMLS | C5848126 | E | validated | |
| MedDRA | 10009868 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98375Autoimmune hemolytic anemia
rare hematological diseases
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/228312
- This record as JSON: /data/d/228312.json