D58.8 Other specified hereditary hemolytic anemias

Billable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.

Applicable to

• Stomatocytosis

Applies from D58 Other hereditary hemolytic anemias

Excludes1 (never code together)

• hemolytic anemia of the newborn (P55.-)

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) 811-812 in MDC 16.

Approximate ICD-9-CM (GEMs)

• 282.8 Other specified hereditary hemolytic anemias

Code annotations containing back-references to D58.8

Back-references to D58

• Type 1 Excludes: D57 Sickle-cell disorders ("other hemoglobinopathies (D58.-)")
• 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 D58.8

• Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hemolytic › hereditary › specified type NEC
• Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hemolytic › specified (hereditary) type NEC
• Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hemolytic › Stransky-Regala type
• Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › stomatocytosis
• Decrease (d) › fragility of erythrocytes
• Stomatocytosis
• Syndrome › hyperviscosity ( of serum) › sclerothymic

Nearby codes

• D58 Other hereditary hemolytic anemias
• D58.0 Hereditary spherocytosis
• D58.1 Hereditary elliptocytosis
• D58.2 Other hemoglobinopathies
• D58.8 Other specified hereditary hemolytic anemias (this code)
• D58.9 Hereditary hemolytic anemia, unspecified