D56.4 - Hereditary persistence of fetal hemoglobin [HPFH]
The ICD 10 Code for Hereditary persistence of fetal hemoglobin [HPFH] is listed as D56.4.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.
| ICD 10 CM Field | Value |
|---|---|
| Diagnosis Code: | D56.4
|
| Description: | Hereditary persistence of fetal hemoglobin [HPFH] |
| Diagnostic Related Groups
(MS-DRG v30.0) |
811 - Red Blood Cell Disorders W Mcc
812 - Red Blood Cell Disorders W/o Mcc |
| Chapter | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) |
| Block | Hemolytic anemias (D55-D59) |
| Parent | D56 - Thalassemia |
| ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD 9 Dx Code: | 282.7 - Other hemoglobinopathies (approximate) |
| ICD-10-CM Siblings (same level / similar specificity) of D56.4: | |
| D56.0 - Alpha thalassemia | |
| D56.1 - Beta thalassemia | |
| D56.2 - Delta-beta thalassemia | |
| D56.3 - Thalassemia minor | |
| D56.5 - Hemoglobin E-beta thalassemia | |
| D56.8 - Other thalassemias | |
| D56.9 - Thalassemia, unspecified | |