Diagnosis Code: D56.4

Short Description: Hereditary persistence of fetal hemoglobin [HPFH]

Long Description: Hereditary persistence of fetal hemoglobin [HPFH]

The code D56.4 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)
    • Thalassemia (D56)
      • D56.4 Hereditary persistence of fetal hemoglobin [HPFH]

Code Version: 2022 ICD-10-CM

Synonyms

• A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis
• Beta plus thalassemia
• Beta plus thalassemia
• Beta plus thalassemia
• Beta zero thalassemia
• Delta beta thalassemia
• Delta beta zero thalassemia
• Hereditary persistence of fetal hemoglobin
• Hereditary persistence of fetal hemoglobin
• Hereditary persistence of fetal hemoglobin delta beta plus thalassemia
• Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia
• Hereditary persistence of fetal hemoglobin thalassemia
• Hereditary persistence of fetal hemoglobin thalassemia
• Hereditary persistence of fetal hemoglobin thalassemia
• Hereditary persistence of fetal hemoglobin thalassemia
• Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome
• HPFH A gamma beta^+^ thalassemia
• HPFH deletion type
• HPFH linked to beta-globulin gene cluster
• HPFH nondeletion type
• HPFH unlinked to beta-globulin gene cluster

Diagnostic Related Group(s)

The code D56.4 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)

Crosswalk Information

Similar Codes

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

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