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The 2025 edition of ICD-10-CM D57.2 became effective on October 1, 2024. This is the American ICD-10-CM version of D57.2 - other international versions of ICD-10 D57.2 may differ. One of the sickle cell disorders characterized by the presence of both hemoglobin s and hemoglobin c.
- D57.40
D57.40 is a billable/specific ICD-10-CM code that can be...
- D57.40
Haemoglobin SC disease is a sickling disorder which results from the co-inheritance of two abnormal ß globin genes, haemoglobin S and haemoglobin C (ß s ß c). It is characterised by the presence of SC poikilocytes, abnormally contracted cells which resemble sickle cells but which have straight edges or are branched.
D57.00 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM D57.00 became effective on October 1, 2024. This is the American ICD-10-CM version of D57.00 - other international versions of ICD-10 D57.00 may differ.
D57.2 is a non-specific and non-billable diagnosis code code, consider using a code with a higher level of specificity for a diagnosis of sickle-cell/hb-c disease. The code is not specific and is NOT valid for the year 2025 for the submission of HIPAA-covered transactions.
Hemoglobin S-C disease is suspected in patients whose clinical features suggest sickle cell disease or whose red blood cells demonstrate sickling. Stained blood smears show target cells, spherocytes, and rarely sickle cells or oat-shaped cells.
4 Οκτ 2022 · Sickle cell disease (SCD) is an inherited group of disorders characterized by the presence of hemoglobin S (Hb S), either from homozygosity for the sickle mutation (Hb SS) or compound heterozygosity with another beta globin variant (eg, sickle-beta thalassemia, Hb SC disease).
Get crucial instructions for accurate ICD-10-CM D57.2 coding with all applicable Excludes 1 and Excludes 2 notes from the section level conveniently shown with each code.
