- D61.01 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM D61.01 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D61.01 – other international versions of ICD-10 D61.01 may differ.
ICD-10-CM D61.01 is grouped within Diagnostic Related Group(s):
- 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
Applicable To
- Blackfan-Diamond syndrome
- Congenital (pure) red cell aplasia
- Familial hypoplastic anemia
- Primary (pure) red cell aplasia
- Red cell (pure) aplasia of infants
Type 1 Excludes
- acquired red cell aplasia (D60.9)
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 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
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to D61.01:
- congenital > red cell (pure) D60.9
- Diamond-Blackfan (congenital hypoplastic) > Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- congenital or familial > hypoplasia, red blood cells D61.9
- congenital or familial (of childhood) > hypoplastic (idiopathic) D61.9
- Joseph-Diamond-Blackfan (congenital hypoplastic) > Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- congenital > pure red cell D60.9
- congenital > bone marrow (myeloid) D61.9
- congenital pure red cell > Aplasia
- erythrocyte congenital > Aplasia
- congenital > red cell (with thymoma) D60.9
- constitutional > red cell (with thymoma) D60.9
- hereditary > red cell (with thymoma) D60.9
- of infants > red cell (with thymoma) D60.9
- primary > red cell (with thymoma) D60.9
- pure > red cell (with thymoma) D60.9
- congenital > Erythroblastopenia D60.9
- erythroid, congenital > Hypoplasia, hypoplastic
- Blackfan-Diamond > Syndrome
- Diamond-Blackfan > Syndrome
- Joseph-Diamond-Blackfan > Syndrome