Diagnosis Code: D58.1

Short Description: Hereditary elliptocytosis

Long Description: Hereditary elliptocytosis

The code D58.1 is VALID for claim submission

Code Classification:

• Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
  • Hemolytic anemias (D55-D59)
    • Other hereditary hemolytic anemias (D58)
      • D58.1 Hereditary elliptocytosis

Code Version: 2022 ICD-10-CM

Synonyms

• Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
• Congenital nephritis
• Elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis
• Hereditary elliptocytosis due to abnormal protein 4.1
• Hereditary elliptocytosis due to alpha spectrin defect
• Hereditary elliptocytosis due to beta spectrin defect in self-association
• Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
• Hereditary elliptocytosis due to deficiency of protein 4.1
• Hereditary elliptocytosis due to glycophorin C deficiency
• Hereditary elliptocytosis with transient poikilocytosis
• Homozygous hereditary elliptocytosis
• Southeast Asian ovalocytosis
• Stomatocytosis

Diagnostic Related Group(s)

The code D58.1 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Red Blood Cell Disorders With Mcc (811)
• Red Blood Cell Disorders Without Mcc (812)

References to Index of Diseases and Injuries

The code D58.1 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Elliptocytosis (congenital)
  • Ovalocytosis (congenital) (hereditary)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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