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ICD-10-CM Codes
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D50-D89
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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D60-D64
Aplastic and other anemias and other bone marrow failure syndromes
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D64-
Other anemias
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2022 ICD-10-CM Diagnosis Code D64.4
2022 ICD-10-CM Diagnosis Code D64.4
Congenital dyserythropoietic anemia
2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- D64.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2022 edition of ICD-10-CM D64.4 became effective on October 1, 2021.
- This is the American ICD-10-CM version of D64.4 - other international versions of ICD-10 D64.4 may differ.
Applicable To- Dyshematopoietic anemia (congenital)
Type 1 ExcludesType 1 Excludes Help
A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as D64.4. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
The following code(s) above
D64.4 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
D64.4:
- Anemia, congenital dyserythropoietic
Clinical Information
- A familial disorder characterized by anemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (erythroid precursor cells). Type ii is the most common of the 3 types; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test.
- A rare congenital anemia caused by mutations in the cdan1 and sec23b genes.
ICD-10-CM D64.4 is grouped within Diagnostic Related Group(s) (MS-DRG v39.0):
- 811 Red blood cell disorders with mcc
- 812 Red blood cell disorders without mcc
Convert D64.4 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
ICD-10-CM Diagnosis Code D64.9
Anemia, unspecified
2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
- congenital P61.4
ICD-10-CM Diagnosis Code P61.4
Other congenital anemias, not elsewhere classified
2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code Code on Newborn Record
- dyserythropoietic, dyshematopoietic D64.4
- dyserythropoietic D64.4 (congenital)
- dyshematopoietic D64.4 (congenital)
ICD-10-CM Codes Adjacent To D64.4
D62 Acute posthemorrhagic anemia
D63 Anemia in chronic diseases classified elsewhere
D63.0 Anemia in neoplastic disease
D63.1 Anemia in chronic kidney disease
D63.8 Anemia in other chronic diseases classified elsewhere
D64.0 Hereditary sideroblastic anemia
D64.1 Secondary sideroblastic anemia due to disease
D64.2 Secondary sideroblastic anemia due to drugs and toxins
D64.3 Other sideroblastic anemias
D64.4
Congenital dyserythropoietic anemia
D64.8 Other specified anemias
D64.81 Anemia due to antineoplastic chemotherapy
D64.89 Other specified anemias
D64.9 Anemia, unspecified
D65 Disseminated intravascular coagulation [defibrination syndrome]
D66 Hereditary factor VIII deficiency
D67 Hereditary factor IX deficiency
D68 Other coagulation defects
D68.0 Von Willebrand's disease
D68.1 Hereditary factor XI deficiency
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
