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)
- acquired red cell aplasia (D60.9)
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)
- neutropenia (D70.-)
Also Known As / Clinical Terms
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
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.