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) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(6)
Related Conditions
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(132)
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
Clinical Terms
- Anemia, dyserythropoietic, congenital
- Giant platelet syndrome
- Congenital dyserythropoietic anemia, type I
- Congenital dyserythropoietic anaemia, type II
- GATA binding protein 1 related thrombocytopenia with dyserythropoiesis
- CDA
- GATA 1 related cytopenia
- X-linked congenital dyserythropoietic anaemia with thrombocytopenia
- ANEMIA DYSERYTHROPOIETIC CONGEN
- X linked macrothrombocytopenia
- Congenital dyserythropoietic anaemia, type III
- Congenital Dyserythropoietic Anemias
- Dyserythropoietic Anemia, Congenital
- Congenital dyserythropoietic anaemia type III
- Congenital dyserythropoietic anaemia, type I
- Congenital hypoplastic anaemia
- Pancreatic insufficiency, dyserythropoietic anaemia, calvarial hyperostosis syndrome
- Dyserythropoietic Anemias, Congenital
- CDA - congenital dyserythropoietic anaemia
- Anemia, Congenital Dyserythropoietic
- Congenital dyserythropoietic anemia, type III
- Dyserythropoietic anemia and thrombocytopenia
- Congenital dyserythropoietic anemia type III
- DYSERYTHROPOIETIC ANEMIA CONGEN
- CIMDAG syndrome
- Congenital dyserythropoietic anaemia
- Congenital dyserythropoietic anemia type I
- Hereditary erythroblast multinuclearity with positive acid serum test
- X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia
- Anemias, Congenital Dyserythropoietic
- Congenital dyserythropoietic anemia (disorder)
- Congenital dyserythropoietic anaemia type I
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation) syndrome
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation syndrome
- Dyshematopoietic anemia (congenital)
- EPI - exocrine pancreatic insufficiency
- Exocrine pancreatic insufficiency
- COX - Cytochrome C oxidase deficiency
- Pancreatic insufficiency
- Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome
- Complex IV deficiency
- ANEMIA CONGEN DYSERYTHROPOIETIC
- Pancreatic exocrine insufficiency
- CONGEN DYSERYTHROPOIETIC ANEMIA
- Cytochrome-c oxidase deficiency
- CDA - congenital dyserythropoietic anemia
- Congenital dyserythropoietic anaemia type 4
- Congenital dyserythropoietic anemia type 4
- Congenital dyserythropoietic anemia, type II
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation) syndrome
- Congenital dyserythropoietic anaemia type IV
- Cytochrome c oxidase deficiency
- Dyserythropoietic anaemia and thrombocytopaenia
- GATA 1 related X linked cytopenia
- Mitochondrial complex IV deficiency
- GATA binding protein 1 related thrombocytopaenia with dyserythropoiesis
- Congenital dyserythropoietic anemia type IV
- X-linked dyserythropoietic anemia with abnormal platelets and neutropenia
- X-linked congenital dyserythropoietic anemia with thrombocytopenia
- HEMPAS - hereditary erythroblast multinuclearity with positive acid serum test
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome
Frequently Asked Questions
What is the ICD-10 code for congenital dyserythropoietic anemia?
The ICD-10-CM code for congenital dyserythropoietic anemia is D64.4. The full clinical description is "Congenital dyserythropoietic anemia". D64.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D64.4 mean?
ICD-10-CM code D64.4 represents “Congenital dyserythropoietic anemia”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and 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.
How does D64.4 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital dyserythropoietic anemia affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D64.4?
D64.4 maps to the ICD-11 code: 3A73 (Congenital dyserythropoietic anaemia).
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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.