D56.8 Other thalassemias
Billable ICD-10-CM code, FY2026.
Applicable to
- Dominant thalassemia
- Hemoglobin C thalassemia
- Mixed thalassemia
- Thalassemia with other hemoglobinopathy
Excludes1 (never code together)
- hemoglobin C disease (D58.2)
- hemoglobin E disease (D58.2)
- other hemoglobinopathies (D58.2)
- sickle-cell anemia (D57.-)
- sickle-cell thalassemia (D57.4-)
Applies from D56 Thalassemia
Excludes1 (never code together)
- sickle-cell thalassemia (D57.4-)
Risk adjustment (HCC)
- CMS-HCC V22: HCC 48 — Coagulation Defects and Other Specified Hematological Disorders
- ESRD V24: HCC 48
MS-DRG index
Defines the logic of DRG(s) 791 in MDC 15.
Approximate ICD-9-CM (GEMs)
Code annotations containing back-references to D56.8
Back-references to D56.8
- Type 1 Excludes:
D58.2 Other hemoglobinopathies ("other hemoglobinopathies with thalassemia (D56.8)")
Back-references to D56
- Code First:
M36.3 Arthropathy in other blood disorders ("thalassemia (D56.-)") - Code First:
M90.5 Osteonecrosis in diseases classified elsewhere ("hemoglobinopathy (D50-D64)") - Type 1 Excludes:
R71 Abnormality of red blood cells ("anemias (D50-D64)")
Diagnosis Index entries for D56.8
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › microcytic (hypochromic) › familial
- Disease, diseased › hemoglobin or Hb › C (Hb-C) › thalassemia
- Hemoglobinopathy (mixed) › with thalassemia
- Thalassemia (anemia) (disease) › with other hemoglobinopathy
- Thalassemia (anemia) (disease) › dominant
- Thalassemia (anemia) (disease) › hemoglobin › C
- Thalassemia (anemia) (disease) › mixed
- Thalassemia (anemia) (disease) › specified type NEC
- Thalassemia (anemia) (disease) › variants
- Variants, thalassemic
Nearby codes
D56.1 Beta thalassemiaD56.2 Delta-beta thalassemiaD56.3 Thalassemia minorD56.4 Hereditary persistence of fetal hemoglobin [HPFH]D56.5 Hemoglobin E-beta thalassemiaD56.8 Other thalassemias (this code)D56.9 Thalassemia, unspecified