ORPHA:275752
Sickle cell disease
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sickle cell disease | |
| fr | Drépanocytose et maladies associées | |
| de | Sichelzellkrankheit | |
| es | Enfermedad falciforme | |
| it | Malattia a cellule falciformi e malattie correlate | |
| nl | Sikkelcelziekte | |
| pt | Anemia falciforme | |
| pl | Niedokrwistość sierpowata i choroby powiązane | |
| cs | Srpkovitá anémie a související nemoci | |
| uk | Серповидноклітинна анемія та повязані з нею захворювання | |
| zh | 镰状细胞病及相关疾病 | |
| tr | Orak hücre hastalığı ve ilgili hastalıklar |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D57.0 | E | specific | validated |
| MONDO | 17146 | E | validated | |
| UMLS | C5680749 | 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:466066Genetic hemoglobinopathy
rare genetic diseases - ORPHA:68364Hemoglobinopathy
rare hematological diseases; rare transplant-related disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:251355OBSOLETE: Sickle cell disease associated with another hemoglobin anomaly referred to · inactive
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/275752
- This record as JSON: /data/d/275752.json