ORPHA:98366
Constitutional hemolytic anemia due to acanthocytosis
Synonyms: Constitutional hemolytic anemia due to acanthocytic disorder
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Constitutional hemolytic anemia due to acanthocytosis | Constitutional hemolytic anemia due to acanthocytic disorder |
| fr | Anémie hémolytique constitutionnelle due à une acanthocytose | Anémie hémolytique constitutionnelle due à une maladie acanthocytique |
| de | Konstitutionelle hämolytische Anämie durch Akanthozytose | |
| es | Anemia hemolítica constitucional por acantocitosis | Anemia hemolítica constitucional por trastorno acantocítico |
| it | Anemia emolitica costituzionale da acantocitosi | Anemia emolitica costituzionale da malattia acantocitica |
| nl | Constitutionele hemolytische anemie als gevolg van acanthocytose | Constitutionele hemolytische anemie als gevolg van een acanthocytische stoornis |
| pt | Acantocitose | |
| pl | Niedokrwistość hemolityczna konstytucjonalna z powodu akantolizy | Dziedzina anemia hemolityczna z powodu akantocytozy |
| cs | Konstituční hemolytická anémie způsobená akantocytózou | = en |
| uk | Конституціональна гемолітична анемія внаслідок акантоцитозу | Конституційна гемолітична анемія внаслідок акантоцитарної недостатності |
| zh | 棘红细胞增多症所致先天性溶血性贫血 | 棘红细胞增多病所致先天性溶血性贫血 |
| tr | Akantositoza bağlı yapısal hemolitik anemi | Akantositik bozukluğa bağlı yapısal hemolitik anemi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 3A10.Y | NTBT | index | validated |
| UMLS | C0687751 | 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:98364Rare constitutional hemolytic anemia due to a red cell membrane anomaly
rare genetic diseases; rare hematological diseases
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/98366
- This record as JSON: /data/d/98366.json