ORPHA:251355
OBSOLETE: Sickle cell disease associated with another hemoglobin anomaly
inactive · referred to ORPHA:275752Sickle cell disease
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Sickle cell disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Sickle cell disease associated with another hemoglobin anomaly | |
| fr | OBSOLETE : Drépanocytose associée à une autre anomalie de l'hémoglobine | |
| de | OBSOLET: Sichelzellkrankheit mit assoziierter weiterer Hämoglobin-Anomalie | |
| es | OBSOLETO: Anemia falciforme asociada a otra anomalía de la hemoglobina | OBSOLETO: Anemia de células falciformes asociada a otra anomalía de la hemoglobina |
| it | OBSOLETO: Drepanocitosi associata ad altro difetto dell'emoglobina | OBSOLETO: Malattia a cellule falciformi con doppia eterozigosi |
| nl | OBSOLEET: Sikkelcelziekte geassocieerd met een andere hemoglobineanomalie | OBSOLEET: Dubbele heterozygote sikkelvorming-stoornis |
| pt | OBSOLETO: Doença de células falciformes associada a outra anomalia da hemoglobina | OBSOLETO: Duplo heterozigoto para doença de falciformação |
| pl | NIEAKTUALNE: Niedokrwistość sierpowata związana z inną anomalią hemoglobiny | |
| cs | NEAKTUÁLNÍ: Srpkovitá anémie asociovaná s dalšími anomáliemi hemoglobinu | NEAKTUÁLNÍ: Srpkovitá porucha dvojích heterozygotů |
| uk | Серповидноклітинна анемія, повязана з іншою аномалією гемоглобіну | Подвійні гетерозиготи серповидної анемії |
| zh | 镰状细胞病相关性其他血红蛋白异常 | 双杂合子镰状形成病症 |
| tr | Başka bir hemoglobin anomalisi ile seyreden orak hücre hastalığı | Çift heterozigot orak hastalığı |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/251355
- This record as JSON: /data/d/251355.json