D61.01
BillableConstitutional (pure) red blood cell aplasia
Constitutional (pure) red blood cell aplasia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Blackfan-Diamond syndrome
- Congenital (pure) red cell aplasia
- Familial hypoplastic anemia
- Primary (pure) red cell aplasia
- Red cell (pure) aplasia of infants
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
- •neutropeniaD70
Related Codes(3)
Also Known As / Clinical Terms(205)
SNOMED CT
- Congenital aplastic anaemia28975000
- Congenital aplastic anemia28975000
- Constitutional aplastic anaemia28975000
- Constitutional aplastic anemia28975000
- Hypoplastic anaemia - familial28975000
- Hypoplastic anemia - familial28975000
- Hypoplastic anaemia41614006
- Hypoplastic anemia41614006
- Primary red cell aplasia50715003
- Pure red cell anaemia50715003
- Pure red cell anemia50715003
- Pure red cell aplasia50715003
- Red cell hypoplasia50715003
- Acute pure red cell anaemia57192008
- Acute pure red cell anemia57192008
- Acute pure red cell aplasia57192008
- Chronic constitutional pure red cell anaemia88854002
- Chronic constitutional pure red cell anemia88854002
- Chronic constitutional pure red cell aplasia88854002
- Congenital erythroid hypoplasia88854002
- Congenital hypoplastic anaemia88854002
- Congenital hypoplastic anemia88854002
- Congenital pure red cell anaemia88854002
- Congenital pure red cell anemia88854002
- Congenital red cell aplasia88854002
- Erythrogenesis imperfecta88854002
- Familial hypoplastic anaemia88854002
- Familial hypoplastic anemia88854002
- Erythroid hypoplasia of bone marrow167923006
- Finding of bone marrow erythropoiesis365835008
UMLS
- ANEMIA HYPOPLASTIC CONGENC0949116
- Anemia, Congenital HypoplasticC0949116
- Anemia, Hypoplastic, CongenitalC0949116
- Anemias, Congenital HypoplasticC0949116
- CONGEN HYPOPLASTIC ANEMIAC0949116
- Congenital Hypoplastic AnemiaC0949116
- Congenital Hypoplastic AnemiasC0949116
- Congenital hypoplastic anemiaC0949116
- Familial hypoplastic anaemiaC0949116
- Familial hypoplastic anemiaC0949116
- HYPOPLASTIC ANEMIA CONGENC0949116
- Hypoplastic Anemia, CongenitalC0949116
- Hypoplastic Anemias, CongenitalC0949116
- Hypoplastic anaemia - familialC0949116
- Hypoplastic anemia - familialC0949116
- congenital hypoplastic anemiaC0949116
- familial hypoplastic anaemiaC0949116
- Anemia, Blackfan DiamondC1260899
- Anemia, Congenital Hypoplastic, Of Blackfan And DiamondC1260899
- Anemia, Diamond BlackfanC1260899
- Anemia, Diamond Blackfan TypeC1260899
- Anemia, Diamond-BlackfanC1260899
- Anemia, Diamond-Blackfan TypeC1260899
- Anemia, Hypoplastic CongenitalC1260899
- Anemias, Hypoplastic CongenitalC1260899
- Blackfan Diamond AnemiaC1260899
- Blackfan Diamond DiseaseC1260899
- Blackfan Diamond SyndromeC1260899
- Blackfan Diamond anemiaC1260899
- Blackfan-Diamond DiseaseC1260899
- Blackfan-Diamond SyndromeC1260899
- Blackfan-Diamond diseaseC1260899
- Blackfan-Diamond syndromeC1260899
- Chronic Congenital Agenerative AnemiaC1260899
- Chronic congenital agenerative anemiaC1260899
- Chronic constitutional pure red cell anaemiaC1260899
- Chronic constitutional pure red cell anemiaC1260899
- Chronic constitutional pure red cell aplasiaC1260899
- Congenital (pure) red cell aplasiaC1260899
- Congenital Anemia, HypoplasticC1260899
- Congenital Anemias, HypoplasticC1260899
- Congenital Erythroid Hypoplastic AnemiaC1260899
- Congenital Hypoplastic Anemia of Blackfan and DiamondC1260899
- Congenital Pure Red Cell AnemiaC1260899
- Congenital Pure Red Cell AplasiaC1260899
- Congenital erythroid hypoplastic anemiaC1260899
- Congenital hypoplastic anaemiaC1260899
- Congenital hypoplastic anemia (disorder)C1260899
- Congenital hypoplastic anemia of Blackfan and DiamondC1260899
- Congenital pure red cell anaemiaC1260899
- Congenital pure red cell anemiaC1260899
- Congenital red cell aplasiaC1260899
- DBAC1260899
- Diamond Anemia, BlackfanC1260899
- Diamond Blackfan AnemiaC1260899
- Diamond-Blackfan AnemiaC1260899
- Diamond-Blackfan Type AnemiaC1260899
- Diamond-Blackfan anaemiaC1260899
- Diamond-Blackfan anemiaC1260899
- Disease, Blackfan-DiamondC1260899
- Erythroblastopenia, InheritedC1260899
- Erythroblastopenias, InheritedC1260899
- Erythrogenesis ImperfectaC1260899
- Erythrogenesis ImperfectasC1260899
- Erythrogenesis imperfectaC1260899
- Hypoplastic Congenital AnemiaC1260899
- Hypoplastic Congenital AnemiasC1260899
- Hypoplastic congenital anemiaC1260899
- Imperfecta, ErythrogenesisC1260899
- Imperfectas, ErythrogenesisC1260899
- Inherited ErythroblastopeniaC1260899
- Inherited ErythroblastopeniasC1260899
- Inherited erythroblastopeniaC1260899
- Pure Hereditary Red Cell AplasiaC1260899
- Pure hereditary red cell aplasiaC1260899
- Red Cell Aplasia, Pure, HereditaryC1260899
- anemia blackfan diamondC1260899
- blackfan diamond anaemiaC1260899
- blackfan diamond anemiaC1260899
- blackfan diamond syndromeC1260899
- blackfan-diamond syndromeC1260899
- diamond blackfan anaemiaC1260899
- diamond blackfan anemiaC1260899
- diamond blackfan syndromeC1260899
- diamond-blackfan anaemiaC1260899
- diamond-blackfan anemiaC1260899
- diamond-blackfan syndromeC1260899
- Constitutional (pure) red blood cell aplasiaC2873778
- Primary (pure) red cell aplasiaC1719320
- Red cell (pure) aplasia of infantsC1719321
Clinical Terms
- Primary (pure) red cell aplasia
- diamond blackfan syndrome
- Anemia, Diamond-Blackfan Type
- Pure Hereditary Red Cell Aplasia
- Congenital pure red cell anaemia
- Hypoplastic anemia - familial
- Congenital Erythroid Hypoplastic Anemia
- blackfan diamond syndrome
- Primary red cell aplasia
- HYPOPLASTIC ANEMIA CONGEN
- Anemia, Diamond-Blackfan
- Red cell (pure) aplasia of infants
- Anemia, Congenital Hypoplastic, Of Blackfan And Diamond
- Anemia, Diamond Blackfan
- Diamond-Blackfan anaemia
- Anemias, Hypoplastic Congenital
- Hypoplastic anaemia
- Acute pure red cell aplasia
- DBA
- Hypoplastic Congenital Anemia
- diamond-blackfan syndrome
- Congenital Hypoplastic Anemias
- Congenital erythroid hypoplasia
- Pure red cell anaemia
- Blackfan Diamond Disease
- ANEMIA HYPOPLASTIC CONGEN
- Chronic constitutional pure red cell anemia
- Blackfan-Diamond syndrome
- Congenital Hypoplastic Anemia
- Red Cell Aplasia, Pure, Hereditary
- Congenital hypoplastic anaemia
- Hypoplastic anemia
- blackfan diamond anaemia
- Blackfan-Diamond Disease
- Congenital Pure Red Cell Aplasia
- Imperfecta, Erythrogenesis
- Erythrogenesis imperfecta
- Blackfan Diamond Anemia
- Hypoplastic Anemia, Congenital
- Anemia, Congenital Hypoplastic
- Hypoplastic Anemias, Congenital
- Finding of bone marrow erythropoiesis
- Congenital red cell aplasia
- Chronic constitutional pure red cell aplasia
- Congenital Anemias, Hypoplastic
- anemia blackfan diamond
- Erythroblastopenias, Inherited
- Constitutional aplastic anemia
- Inherited Erythroblastopenia
- Familial hypoplastic anaemia
- Congenital Hypoplastic Anemia of Blackfan and Diamond
- Anemia, Hypoplastic, Congenital
- Anemias, Congenital Hypoplastic
- Chronic Congenital Agenerative Anemia
- diamond blackfan anaemia
- Erythroid hypoplasia of bone marrow
- Disease, Blackfan-Diamond
- Congenital Pure Red Cell Anemia
- Acute pure red cell anemia
- Pure red cell anemia
- Pure red cell aplasia
- Anemia, Hypoplastic Congenital
- Diamond-Blackfan anemia
- Diamond Anemia, Blackfan
- Diamond-Blackfan Type Anemia
- Familial hypoplastic anemia
- Hypoplastic Congenital Anemias
- CONGEN HYPOPLASTIC ANEMIA
- Anemia, Blackfan Diamond
- Erythrogenesis Imperfectas
- Imperfectas, Erythrogenesis
- Acute pure red cell anaemia
- Constitutional aplastic anaemia
- Congenital hypoplastic anemia (disorder)
- Congenital Anemia, Hypoplastic
- Congenital aplastic anaemia
- Diamond Blackfan Anemia
- Chronic constitutional pure red cell anaemia
- Red cell hypoplasia
- Erythroblastopenia, Inherited
- Congenital (pure) red cell aplasia
- Anemia, Diamond Blackfan Type
- Inherited Erythroblastopenias
- Hypoplastic anaemia - familial
- Congenital aplastic anemia
Frequently Asked Questions
What is the ICD-10 code for constitutional (pure) red blood cell aplasia?
The ICD-10-CM code for constitutional (pure) red blood cell aplasia is D61.01. The full clinical description is "Constitutional (pure) red blood cell aplasia". D61.01 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D61.01 mean?
ICD-10-CM code D61.01 represents “Constitutional (pure) red blood cell aplasia”. 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 D61.01 a billable code?
Yes, D61.01 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D61.01 in?
D61.01 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D61.01?
D61.01 has Excludes1 notes indicating codes that cannot be used together with it, including: acquired red cell aplasia (D60.9).
What SNOMED CT codes does D61.01 map to?
D61.01 maps to 7 SNOMED CT concepts: 57192008, 88854002, 28975000, 167923006, 365835008, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D61.01?
D61.01 is linked to 5 UMLS Concept Unique Identifiers: C0949116, C1260899, C2873778, C1719320, C1719321. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D61.01 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like constitutional (pure) red blood cell aplasia 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 D61.01?
There is no direct ICD-11 mapping available for D61.01 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.