D58.1
D58.1: Hereditary elliptocytosis
Billable / specific codeICD-10-CM
D58.1 is a billable, specific ICD-10-CM code for hereditary elliptocytosis. It is valid for submission on a claim.
Check D58.1 with the rest of the claim: free scrubberInclusion terms
Alternative wordings a physician may use in the chart for this same code.
- Elliptocytosis (congenital)
- Ovalocytosis (congenital) (hereditary)
Other codes that can never be billed with D58.1
Their own Excludes1 notes name this code, so the conflict is not listed above.
Risk adjustment
No CMS-HCC V28 category: this code does not change a RAF score.
Medicare coverage
D58.1 is named in 8 Medicare coverage policies: 8 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A55717Billing and Coding: Lab: Flow Cytometry
- A56464Billing and Coding: Flow Cytometry
- A56718Billing and Coding: Intravenous Immunoglobulin (IVIG)
- A57110Billing and Coding: MolDX: Blood Product Molecular Antigen Typing
Alphabetic index entries that lead here
- Dresbach's syndrome(elliptocytosis)
- Elliptocytosis(congenital) (hereditary)
- Elliptocytosis›Hb C(disease)
- Elliptocytosis›hemoglobin disease
- Syndrome›Dresbach's(elliptocytosis)
- Disease, diseased›hemoglobin or Hb›elliptocytosis
- Disease, diseased›hemoglobin or Hb›C›elliptocytosis
Code history
Unchanged in every release from FY2024 to FY2027.