ORPHA:98362
Constitutional sideroblastic anemia
- 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 sideroblastic anemia | |
| fr | Anémie sidéroblastique constitutionnelle | |
| de | Anämie, konstitutionelle sideroblastische | |
| es | Anemia sideroblástica constitucional | |
| it | Anemia sideroblastica costituzionale | |
| nl | Constitutionele sideroblastische anemie | |
| pt | Anemia sideroblástica genética | |
| pl | Niedokrwistość sideroblastyczna konstytucjonalna | |
| cs | Konstituční sideroblastické anémie | |
| uk | Конституційна сидеробластна анемія | |
| zh | 原发性铁粒幼细胞性贫血 | |
| tr | Yapısal sideroblastik anemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D64.0 | E | specific | validated |
| ICD-11 | 3A72.0 | E | specific | validated |
| UMLS | C0221018 | 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 (2):
- ORPHA:183651Rare constitutional anemia
rare genetic diseases - ORPHA:1047Sideroblastic anemia
rare hematological diseases
Children (9):
- ORPHA:255132Adult-onset autosomal recessive sideroblastic anemia
- ORPHA:260305Autosomal recessive sideroblastic anemia
- ORPHA:369861Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
- ORPHA:2598Mitochondrial myopathy and sideroblastic anemia
- ORPHA:699Pearson syndrome
- ORPHA:300298Severe congenital hypochromic anemia with ringed sideroblasts
- ORPHA:49827Thiamine-responsive megaloblastic anemia syndrome
- ORPHA:75563X-linked sideroblastic anemia
- ORPHA:2802X-linked sideroblastic anemia and spinocerebellar ataxia
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98362
- This record as JSON: /data/d/98362.json