ORPHA:398109
Neonatal autoimmune hemolytic anemia
Synonyms: Neonatal AHA · Neonatal AIHA
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Neonatal
- Status
- active
A rare, secondary, neonatal autoimmune disease characterized by onset of hemolytic anemia in the neonatal period associated with a positive direct antiglobulin test. Hepatosplenomegaly may be associated.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neonatal autoimmune hemolytic anemia | Neonatal AHA · Neonatal AIHA |
| fr | Anémie hémolytique auto-immune néonatale | AHA néonatale · AHAI néonatale · AIHA néonatale |
| de | Neonatale autoimmune hämolytische Anämie | Neonatales AHA · Neonatales AIHA |
| es | Anemia hemolítica autoinmune neonatal | AHA neonatal · AIHA neonatal |
| it | Anemia emolitica autoimmune neonatale | AHA neonatale · AIHA neonatale |
| nl | Neonatale auto-immune hemolytische anemie | Neonatale AHA · Neonatale AIHA |
| pt | Anemia hemolítica autoimune neonatal | |
| pl | Autoimmunologiczna niedokrwistość hemolityczna noworodków | AHA noworodków · AIHA noworodków |
| cs | Neonatální AIHA | Neonatální AHA · Neonatální autoimunitní hemolytická anémie |
| uk | Неонатальна аутоімунна гемолітична анемія | Неонатальний AHA · Неонатальний AIHA |
| zh | 新生儿自身免疫性溶血性贫血 | 新生儿AIHA |
| tr | Yenidoğan otoimmün hemolitik anemisi | Yenidoğan AHA · Yenidoğan AIHA |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D59.1 | NTBT | attributed | validated |
| ICD-11 | 3A20.Y | NTBT | attributed | validated |
| MONDO | 0018358 | E | validated | |
| UMLS | C4751517 | 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:398091Secondary neonatal autoimmune disease
rare systemic and rheumatological diseases; rare systemic or rheumatologic diseases of childhood
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 2 cases | Worldwide | Case(s) | Validated | 12819171[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET_12819171[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/398109
- This record as JSON: /data/d/398109.json