ORPHA:707786
Thalassemia
- 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.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Thalassemia | |
| fr | Thalassémie | |
| de | Thalassämie | |
| es | Talasemia | |
| it | Talassemia | |
| nl | Thalassemie | |
| pt | Thalassemia | |
| pl | Talasemia | |
| cs | Thalassemia |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:466066Genetic hemoglobinopathy
rare genetic diseases - ORPHA:68364Hemoglobinopathy
rare hematological diseases; rare transplant-related disorders
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/707786
- This record as JSON: /data/d/707786.json