Alphabetic Index · main term
Leptocytosis, hereditary
Leptocytosis, hereditary is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists D56.9 for this term: Thalassemia, unspecified. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Thalassemia, unspecified
Other Index terms that lead to D56.9
Different words, same code. 11 entries
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), Mediterranean (with other hemoglobinopathy)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), microelliptopoikilocytic (Rietti-Greppi- Micheli)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), Rietti-Greppi-Micheli
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), thalassemia
- Arthritis, arthritic (acute) (chronic) (nonpyogenic) (subacute), in (due to), thalassemia NEC
- Disease, diseased, hemoglobin or Hb, abnormal (mixed) NEC, with thalassemia
- Disease, diseased, hemoglobin or Hb, H (Hb-H) (thalassemia), with other abnormal hemoglobin NEC
- Disease, diseased, hemoglobin or Hb, I thalassemia
- Disease, diseased, high fetal gene or hemoglobin thalassemia
- Rietti-Greppi-Micheli anemia
- Thalassemia (anemia) (disease)