D56.4 - Hereditary persistence of fetal hemoglobin [HPFH]

  • Applicable to Hereditary persistence of fetal hemoglobin [HPFH]
  • The 2025 edition of ICD10-CM D56.4 became effective on October 1, 2024.
  • This is the American ICD10-CM version of D56.4 - other international versions of ICD10 D56.4 may differ.
  • D56.4 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

The following codes above D56.4 contain annotation back-references that may be applicable to D56.4:

Chapter: D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Section: D55-D59 Hemolytic anemias

Category: D56 Thalassemia

disorders icd 10
 
hereditary icd 10
 
thalassemia icd 10
 
blood icd 10
 
immune icd 10
 
hpfh icd 10
 
fetal icd 10
 
hemoglobin icd 10
 
hemolytic icd 10
 
mechanism icd 10
 
persistence icd 10
 
anemias icd 10
 
organs icd 10
 
Billable/Specific Code

Browse other similar CM codes

D56.0
 
D56.1
 
D56.2
 
D56.3
 
D56.4
 
D56.5
 
D56.8
 
D56.9
 

Please, give attribution to our website icd-10code.com