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Sickle cell disease (SCD), also simply called sickle cell, is a group of inherited hemoglobin-related blood disorders. Sickle cell disease is caused by an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. This leads to the red blood cells adopting an abnormal sickle-like shape under certain circumstances. With this shape…
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| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Sickle cell disease | Causes | Genetic: inherited HBB gene mutation | 1.00 | infobox |
| Sickle cell disease | Complications | Chronic pain, stroke, aseptic bone necrosis, gallstones, leg ulcers, priapism, pulmonary hypertension, vision problems, kidney problems | 1.00 | infobox |
| Sickle cell disease | Deaths | 34,000 p.a. (a contributory factor to a further 376,000 p.a.) | 1.00 | infobox |
| Sickle cell disease | Diagnostic method | Blood test | 1.00 | infobox |
| Sickle cell disease | Frequency | 7.7 million (2021) | 1.00 | infobox |
| Sickle cell disease | Other names | Sickle cell disorder; drepanocytosis (dated) | 1.00 | infobox |
| Sickle cell disease | Prognosis | Life expectancy 40–60 years (developed world) | 1.00 | infobox |
| Sickle cell disease | Risk factors | Ancestry from sub-Saharan Africa, India, the Arab Gulf states or Sicily | 1.00 | infobox |
| Sickle cell disease | Specialty | Haematology, medical genetics | 1.00 | infobox |
| Sickle cell disease | Symptoms | Attacks of pain, anaemia, swelling in the hands and feet, bacterial infections, stroke | 1.00 | infobox |
| Sickle cell disease | Treatment | Vaccination, antibiotics, high fluid intake, folic acid supplementation, pain medication, blood transfusions | 1.00 | infobox |
| Sickle cell disease | Usual onset | 5–6 months of age | 1.00 | infobox |
| Sickle cell disease | is a | most common genetic disorder among African Americans | 0.90 | text |
| Sickle cell disease | is a | genetic disease | 0.90 | text |
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