ICD-10-CM Code D56.4
Hereditary persistence of fetal hemoglobin [HPFH]
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
D56.4 is a billable ICD code used to specify a diagnosis of hereditary persistence of fetal hemoglobin [HPFH]. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code D564 is used to code Hereditary persistence of fetal hemoglobin
Hereditary persistence of fetal hemoglobin (HPFH, BrE: Hereditary persistence of foetal haemoglobin) is a benign condition in which significant fetal hemoglobin (hemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult-type hemoglobin should be produced.
|ICD 9 Code:||282.7|
- DRG Group #811-812 - Red blood cell disorders with MCC.
- DRG Group #811-812 - Red blood cell disorders without MCC.
Related Concepts SNOMET-CT
- Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder)
- Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia (disorder)
ICD-10-CM Alphabetical Index References for 'D56.4 - Hereditary persistence of fetal hemoglobin [HPFH]'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D56.4. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code D56.4 and a single ICD9 code, 282.7 is an approximate match for comparison and conversion purposes.