D56.4
BillableHereditary persistence of fetal hemoglobin [HPFH]
Hereditary persistence of fetal hemoglobin [HPFH]
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- sickle-cell thalassemia (D57.4-)
Excludes 2
Conditions not included here, but the patient may have both
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis5967006
- A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis5967006
- A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis5967006
- Delta beta thalassaemia16360009
- Delta beta thalassemia16360009
- Delta-beta thalassaemia16360009
- Delta-beta thalassemia16360009
- F thalassaemia16360009
- F thalassemia16360009
- HPFH (hereditary persistence of fetal haemoglobin) beta-thalassaemia syndrome16964007
- HPFH (hereditary persistence of fetal hemoglobin) beta-thalassemia syndrome16964007
- Hereditary persistence of fetal haemoglobin thalassaemia16964007
- Hereditary persistence of fetal hemoglobin thalassemia16964007
- Hereditary persistence of foetal haemoglobin thalassaemia16964007
- HPFH unlinked to beta-globulin gene cluster32855007
- Hereditary persistence of fetal haemoglobin unlinked to beta-globulin gene cluster32855007
- Hereditary persistence of fetal hemoglobin (HPF) unlinked to beta-globulin gene cluster32855007
- Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster32855007
- Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster32855007
- HPFH A gamma beta^+^ thalassaemia39586009
- HPFH A gamma beta^+^ thalassemia39586009
- Hereditary persistence of fetal haemoglobin A gamma beta^+^ thalassaemia39586009
- Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia39586009
- Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia39586009
- Hereditary persistence of foetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia39586009
- HPFH (hereditary persistence of fetal haemoglobin) delta beta plus thalassaemia54006005
- HPFH (hereditary persistence of fetal hemoglobin) delta beta plus thalassemia54006005
- HPFH (hereditary persistence of foetal haemoglobin) delta beta plus thalassaemia54006005
- Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia54006005
- Hereditary persistence of fetal hemoglobin delta beta plus thalassemia54006005
- Hereditary persistence of foetal haemoglobin delta beta plus thalassaemia54006005
- HPFH nondeletion type56205004
- Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type56205004
- Hereditary persistence of fetal hemoglobin, nondeletion type56205004
- Hereditary persistence of foetal haemoglobin (HPFH) nondeletion type56205004
- HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia61395005
- HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia61395005
- HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia61395005
- Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia61395005
- Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia61395005
- Delta beta zero thalassaemia76336008
- Delta beta zero thalassemia76336008
- Beta plus thalassaemia79592006
- Beta plus thalassemia79592006
- beta plus thalassaemia79592006
- beta plus thalassemia79592006
- HPFH deletion type85557000
- Hereditary persistence of fetal haemoglobin deletion type85557000
- Hereditary persistence of fetal hemoglobin (HPFH) deletion type85557000
- Hereditary persistence of fetal hemoglobin deletion type85557000
- Hereditary persistence of foetal haemoglobin (HPFH) deletion type85557000
- Beta 0 thalassaemia86715000
- Beta 0 thalassemia86715000
- Beta zero thalassaemia86715000
- Beta zero thalassemia86715000
- beta zero thalassaemia86715000
- beta zero thalassemia86715000
- HPFH linked to beta-globulin gene cluster89459006
- Hereditary persistence of fetal haemoglobin (HPFH) linked to beta-globulin gene cluster89459006
- Hereditary persistence of fetal haemoglobin linked to beta-globulin gene cluster89459006
- Hereditary persistence of fetal hemoglobin (HPFH) linked to beta-globulin gene cluster89459006
- Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster89459006
- Hereditary persistence of foetal haemoglobin (HPFH) linked to beta-globulin gene cluster89459006
- HPFH - Hereditary persistence of fetal haemoglobin191201002
- HPFH - Hereditary persistence of fetal hemoglobin191201002
- HPFH - Hereditary persistence of foetal haemoglobin191201002
- Hb F disease191201002
- Hereditary persistence of fetal haemoglobin191201002
- Hereditary persistence of fetal hemoglobin191201002
- Hereditary persistence of foetal haemoglobin191201002
- Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome783254003
- Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome783254003
- Dias Logan syndrome1360079000
- Hereditary persistence of fetal haemoglobin, intellectual disability syndrome1360079000
- Hereditary persistence of fetal hemoglobin, intellectual disability syndrome1360079000
- Hereditary persistence of foetal haemoglobin, intellectual disability syndrome1360079000
UMLS
- Disease, Hemoglobin FC0019025
- HEMOGLOBIN F DISC0019025
- HEREDITARY PERSISTENCE OF FETAL HEMOGLOBINC0019025
- HPFH (hereditary persistence of fetal hemoglobin)C0019025
- HPFH - Hereditary persistence of fetal haemoglobinC0019025
- HPFH - Hereditary persistence of fetal hemoglobinC0019025
- HPFH - Hereditary persistence of foetal haemoglobinC0019025
- Hb F diseaseC0019025
- Hemoglobin F DiseaseC0019025
- Hereditary Persistence of Fetal HemoglobinC0019025
- Hereditary persistence of fetal haemoglobinC0019025
- Hereditary persistence of fetal hemoglobinC0019025
- Hereditary persistence of fetal hemoglobin (disorder)C0019025
- Hereditary persistence of fetal hemoglobin [HPFH]C0019025
- Hereditary persistence of foetal haemoglobinC0019025
- hereditary persistence of fetal hemoglobinC0019025
Frequently Asked Questions
What is ICD-10 code D56.4?
ICD-10-CM code D56.4 represents "Hereditary persistence of fetal hemoglobin [HPFH]". It is a billable/specific code that can be used on a claim.
Is D56.4 a billable code?
Yes, D56.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D56.4 in?
D56.4 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D56.4?
D56.4 has Excludes1 notes indicating codes that cannot be used together with it, including: sickle-cell thalassemia (D57.4-).
What SNOMED CT codes does D56.4 map to?
D56.4 maps to 16 SNOMED CT concepts: 5967006, 86715000, 79592006, 16360009, 76336008, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D56.4?
D56.4 is linked to 1 UMLS Concept Unique Identifier: C0019025. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.