Sickle cell disease
ICD-10 Code
D57
Category
Hematologic
Sickle cell disease
Definition
Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur.
Also known as Haemoglobin S disease without crisis, Hb-S/Hb-C disease, sickle cell anemia, Sickle Cell Disease, sickle-cell/Hb-C disease without crisis, sickling disorder due to Haemoglobin S, sickling disorder due to Hemoglobin S — per MONDO
Also identified as
- DOID 0081445 per MONDO
- DOID 10923 per MONDO
- ICD10CM D57.2 per MONDO
- ICD9 282.6 per MONDO
- ICD9 282.60 per MONDO
- ICD9 282.63 per MONDO
- MESH D000755 per MONDO
- NCIT C34383 per MONDO
- OMIM 603903 per MONDO
- Orphanet 232 per MONDO
- UMLS C0002895 per MONDO
Drugs indicated
| Drug | Relation | Source |
|---|---|---|
| Exagamglogene Autotemcel | may treat | MEDRT · Public domain (U.S. Government work) |