1. ICD-10-CM Codes
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2. D50-D89
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3. D60-D64
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4. D61-
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5. 2023 ICD-10-CM Diagnosis Code D61.09

2023 ICD-10-CM Diagnosis Code D61.09

Other constitutional aplastic anemia

2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

• D61.09 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
• The 2023 edition of ICD-10-CM D61.09 became effective on October 1, 2022.
• This is the American ICD-10-CM version of D61.09 - other international versions of ICD-10 D61.09 may differ.

• Anemia, fanconi
• Fanconi's anemia

• A rare inherited disorder in which the bone marrow does not make blood cells. It is usually diagnosed in children between 2 and 15 years old. Symptoms include frequent infections, easy bleeding, and extreme tiredness. People with fanconi anemia may have a small skeleton and brown spots on the skin. They also have an increased risk of developing certain types of cancer.
• An autosomal recessive genetic disorder characterized by bone marrow failure, skeletal abnormalities, and an increase incidence of development of neoplasias.
• Congenital disorder affecting all bone marrow elements, resulting in anemia; leukopenia; and thrombopenia, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous chromosome breakage is a feature of this disease along with predisposition to leukemia. There are at least 7 complementation groups in fanconi anemia: fanca, fancb, fancc, fancd1, fancd2, fance, fancf, fancg, and fancl. (from online mendelian inheritance in man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, august 20, 2004)

• 808 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders with mcc
• 809 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders with cc
• 810 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders without cc/mcc

Convert D61.09 to ICD-9-CM

• 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
• 2023 (effective 10/1/2022): No change

• Type 1 Excludes: E79
  ICD-10-CM Diagnosis Code E79

  Disorders of purine and pyrimidine metabolism

  2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code

  Type 1 Excludes

  • Ataxia-telangiectasia (Q87.19)
  • Bloom's syndrome (Q82.8)
  • Cockayne's syndrome (Q87.19)
  • calculus of kidney (N20.0)
  • combined immunodeficiency disorders (D81.-)
  • Fanconi's anemia (D61.09)
  • gout (M1A.-, M10.-)
  • orotaciduric anemia (D53.0)
  • progeria (E34.8)
  • Werner's syndrome (E34.8)
  • xeroderma pigmentosum (Q82.1)

• Aleukia
  • hemorrhagica D61.9
    ICD-10-CM Diagnosis Code D61.9

    Aplastic anemia, unspecified

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Hypoplastic anemia NOS
    • Medullary hypoplasia
    • congenital D61.09
• 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 2023 Billable/Specific Code
  • aplastic D61.9
    ICD-10-CM Diagnosis Code D61.9

    Aplastic anemia, unspecified

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Hypoplastic anemia NOS
    • Medullary hypoplasia
    • congenital D61.09
  • aregenerative
    • congenital D61.09
  • congenital P61.4
    ICD-10-CM Diagnosis Code P61.4

    Other congenital anemias, not elsewhere classified

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Code on Newborn Record

    Applicable To

    • Congenital anemia NOS
    • aplastic D61.09
  • chronica congenita aregenerativa D61.09
  • Fanconi's D61.09 (congenital pancytopenia)
• Disease, diseased - see also Syndrome
  • Fanconi's D61.09 (congenital pancytopenia)
• Erythroblastophthisis D61.09
• Erythrogenesis imperfecta D61.09
• Fanconi's anemia D61.09 (congenital pancytopenia)
• Pancytopenia (acquired) D61.818
  ICD-10-CM Diagnosis Code D61.818

  Other pancytopenia

  2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • with
    • malformations D61.09
  • congenital D61.09
• Panhematopenia D61.9
  ICD-10-CM Diagnosis Code D61.9

  Aplastic anemia, unspecified

  2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

  Applicable To

  • Hypoplastic anemia NOS
  • Medullary hypoplasia
  • congenital D61.09
  • constitutional D61.09
• Panhemocytopenia D61.9
  ICD-10-CM Diagnosis Code D61.9

  Aplastic anemia, unspecified

  2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

  Applicable To

  • Hypoplastic anemia NOS
  • Medullary hypoplasia
  • congenital D61.09
  • constitutional D61.09
• Panmyelopathy, familial, constitutional D61.09
• Panmyelophthisis D61.82
  ICD-10-CM Diagnosis Code D61.82

  Myelophthisis

  2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

  Applicable To

  • Leukoerythroblastic anemia
  • Myelophthisic anemia
  • Panmyelophthisis

  Code Also

  • the underlying disorder, such as:
  • malignant neoplasm of breast (C50.-)
  • tuberculosis (A15.-)

  Type 1 Excludes

  • idiopathic myelofibrosis (D47.1)
  • myelofibrosis NOS (D75.81)
  • myelofibrosis with myeloid metaplasia (D47.4)
  • primary myelofibrosis (D47.1)
  • secondary myelofibrosis (D75.81)
  • congenital D61.09
• Syndrome - see also Disease
  • Fanconi's D61.09 (anemia) (congenital pancytopenia)

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.