D64.4
BillableCongenital dyserythropoietic anemia
Congenital dyserythropoietic anemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Dyshematopoietic anemia (congenital)
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
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
- Congenital dyserythropoietic anaemia type III26409005
- Congenital dyserythropoietic anaemia, type III26409005
- Congenital dyserythropoietic anemia type III26409005
- Congenital dyserythropoietic anemia, type III26409005
- Pancreatic insufficiency37992001
- EPI - exocrine pancreatic insufficiency47367009
- Exocrine pancreatic insufficiency47367009
- Pancreatic exocrine insufficiency47367009
- CDA - congenital dyserythropoietic anaemia52951008
- CDA - congenital dyserythropoietic anemia52951008
- Congenital dyserythropoietic anaemia52951008
- Congenital dyserythropoietic anemia52951008
- Congenital dyserythropoietic anaemia type I59548005
- Congenital dyserythropoietic anaemia, type I59548005
- Congenital dyserythropoietic anemia type I59548005
- Congenital dyserythropoietic anemia, type I59548005
- COX - Cytochrome C oxidase deficiency67434000
- Complex IV deficiency67434000
- Cytochrome c oxidase deficiency67434000
- Cytochrome-c oxidase deficiency67434000
- Mitochondrial complex IV deficiency67434000
- Congenital dyserythropoietic anaemia, type II68870007
- Congenital dyserythropoietic anemia, type II68870007
- HEMPAS - hereditary erythroblast multinuclearity with positive acid serum test68870007
- Hereditary erythroblast multinuclearity with positive acid serum test68870007
- Giant platelet syndrome234478007
- Dyserythropoietic anaemia and thrombocytopaenia713388002
- Dyserythropoietic anemia and thrombocytopenia713388002
- GATA 1 related X linked cytopenia713388002
- GATA 1 related cytopenia713388002
- GATA binding protein 1 related thrombocytopaenia with dyserythropoiesis713388002
- GATA binding protein 1 related thrombocytopenia with dyserythropoiesis713388002
- X linked macrothrombocytopenia713388002
- Congenital dyserythropoietic anaemia type 4719453009
- Congenital dyserythropoietic anaemia type IV719453009
- Congenital dyserythropoietic anemia type 4719453009
- Congenital dyserythropoietic anemia type IV719453009
- Pancreatic insufficiency, dyserythropoietic anaemia, calvarial hyperostosis syndrome722207000
- Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome722207000
- X-linked congenital dyserythropoietic anaemia with thrombocytopenia722475006
- X-linked congenital dyserythropoietic anemia with thrombocytopenia722475006
- X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia782759001
- X-linked dyserythropoietic anemia with abnormal platelets and neutropenia782759001
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation) syndrome1332508004
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation) syndrome1332508004
- CIMDAG syndrome1332508004
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation syndrome1332508004
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome1332508004
UMLS
- ANEMIA CONGEN DYSERYTHROPOIETICC0002876
- ANEMIA DYSERYTHROPOIETIC CONGENC0002876
- Anemia, Congenital DyserythropoieticC0002876
- Anemia, Dyserythropoietic, CongenitalC0002876
- Anemia, dyserythropoietic, congenitalC0002876
- Anemias, Congenital DyserythropoieticC0002876
- CDAC0002876
- CDA - congenital dyserythropoietic anaemiaC0002876
- CDA - congenital dyserythropoietic anemiaC0002876
- CONGEN DYSERYTHROPOIETIC ANEMIAC0002876
- Congenital Dyserythropoietic AnemiaC0002876
- Congenital Dyserythropoietic AnemiasC0002876
- Congenital dyserythropoietic anaemiaC0002876
- Congenital dyserythropoietic anemiaC0002876
- Congenital dyserythropoietic anemia (disorder)C0002876
- Congenital hypoplastic anaemiaC0002876
- DYSERYTHROPOIETIC ANEMIA CONGENC0002876
- Dyserythropoietic Anemia, CongenitalC0002876
- Dyserythropoietic Anemias, CongenitalC0002876
- Dyshematopoietic anemia (congenital)C0002876
- cdaC0002876
- congenital dyserythropoietic anaemiaC0002876
- congenital dyserythropoietic anemiaC0002876
Frequently Asked Questions
What is ICD-10 code D64.4?
ICD-10-CM code D64.4 represents "Congenital dyserythropoietic anemia". It is a billable/specific code that can be used on a claim.
Is D64.4 a billable code?
Yes, D64.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D64.4 in?
D64.4 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D64.4?
D64.4 has Excludes1 notes indicating codes that cannot be used together with it, including: refractory anemia (D46.-); refractory anemia with excess blasts in transformation [RAEB T] (C92.0-); Blackfan-Diamond syndrome (D61.01); and 1 more.
What SNOMED CT codes does D64.4 map to?
D64.4 maps to 14 SNOMED CT concepts: 52951008, 1332508004, 67434000, 719453009, 59548005, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D64.4?
D64.4 is linked to 1 UMLS Concept Unique Identifier: C0002876. 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.