D58.0 Hereditary spherocytosis
The ICD-10-CM code for Hereditary spherocytosis is D58.0 (FY2026). It is a billable, claim-ready diagnosis code.
Classification
- Section
- D55-D59: Hemolytic anemias (D55-D59)
- Category D58
- 6 codes (5 billable)
- FY2026 Status
- Stable since FY2024
Also Known As
ICD-10-CM Alphabetic Index entries that lead to D58.0:
- Spherocytosis (congenital) (familial) (hereditary)
- Syndrome › Minkowski-Chauffard
- Spherocytosis (congenital) (familial) (hereditary) › hemoglobin disease
- Jaundice (yellow) › newborn › spherocytosis (congenital)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › congenital › spherocytic
- Disease, diseased › hemoglobin or Hb › spherocytosis
Inclusion Terms
- Acholuric (familial) jaundice
- Congenital (spherocytic) hemolytic icterus
- Minkowski-Chauffard syndrome
U.S. Hospital Utilization
- An estimated 3,830 U.S. inpatient stays in 2023 included D58.0 among the documented diagnoses.
- 525 stays listed it as the principal diagnosis.
Source: National Inpatient Sample (NIS), Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, 2016–2023. National survey-weighted estimates.
Official Coding Guidelines
Chapter 3 TOC entry3. Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) ............................................................................................. 39
Reserved for future guideline expansionReserved for future guideline expansion ...................................................................................... 39
Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026