ORPHA:293830
Constitutional dyserythropoietic anemia
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Infancy, Neonatal
- 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 | Constitutional dyserythropoietic anemia | |
| fr | Anémie dysérythropoïétique constitutionnelle | |
| de | Konstitutionelle dyserythropoetische Anämie | |
| es | Anemia diseritropoyética constitucional | |
| it | Anemia diseritropoietica costituzionale | |
| nl | Constitutionele dyserytropoëtische anemie | |
| pt | Anemia diseritropoiética constitucional | |
| pl | Niedokrwistość dyserytropoetyczna konstytucjonalna | |
| cs | Konstituční dyserytropoetická anémie | |
| uk | Конституційна дизеритропоетична анемія | |
| zh | 体质性红细胞生成障碍性贫血 | |
| tr | Yapısal dizeritropoietik anemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17397 | E | validated | |
| UMLS | C5680998 | 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 (2):
- ORPHA:108997Rare anemia
rare hematological diseases - ORPHA:183651Rare constitutional anemia
rare genetic diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/293830
- This record as JSON: /data/d/293830.json