ICD-10-CM 2027 diagnosis code
D61.01Constitutional (pure) red blood cell aplasia
D61.01 is a valid, billable ICD-10-CM code for constitutional (pure) red blood cell aplasia. It can be reported on claims for dates of service from October 1, 2026 – September 30, 2027.
Looking up by condition? See ICD-10 code for Kaznelson's syndrome, ICD-10 code for Diamond-Blackfan anemia, ICD-10 code for Joseph-Diamond-Blackfan anemia, ICD-10 code for Blackfan-Diamond anemia or syndrome.
Code unchanged since ICD-10-CM took effect on October 1, 2015. Source: official FY2027 ICD-10-CM release from CDC/NCHS and CMS. Page updated September 29, 2026. About our data
About D61.01
D61.01 is the ICD-10-CM diagnosis code for constitutional (pure) red blood cell aplasia. It belongs to category D61 (other aplastic anemias and other bone marrow failure syndromes), block D60-D64 (aplastic and other anemias and other bone marrow failure syndromes) and chapter 3 (diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism). It is billable, so it can be reported on its own for dates of service from October 1, 2026 through September 30, 2027.
Within D61.0 (constitutional aplastic anemia), D61.01 is specifically for constitutional (pure) red blood cell aplasia. Related codes cover Shwachman-Diamond syndrome (D61.02), Fanconi anemia (D61.03) and other constitutional aplastic anemia (D61.09).
Don't report D61.01 together with the conditions in its Excludes1 note: acquired red cell aplasia (D60.9).
As a secondary diagnosis it is a CC (complication or comorbidity), which can move an inpatient stay into the "with CC" MS-DRG of its family, unless the principal diagnosis excludes it.
In MS-DRG v44.0, it is part of the grouping logic for DRG 808 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCC, relative weight 2.1705), DRG 809 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CC, relative weight 1.2262) and DRG 810 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCC, relative weight 1.075), in MDC 16 (Diseases and Disorders of the Blood and Blood Forming Organs and Immunological Disorders), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.
It has been part of ICD-10-CM since the code set took effect on October 1, 2015 and hasn't changed since.
Before ICD-10, this condition was coded in ICD-9-CM as 284.01 (constitutional red blood cell aplasia).
Coding notes
- Blackfan-Diamond syndrome
- Congenital (pure) red cell aplasia
- Familial hypoplastic anemia
- Primary (pure) red cell aplasia
- Red cell (pure) aplasia of infants
- acquired red cell aplasia (D60.9)
Notes that apply from higher levels
Instructions written at a parent level also apply to D61.01.
› From D61 Other aplastic anemias and other bone marrow failure syndromes
- neutropenia (D70.-)
Broader instructions also apply from Chapter 3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
Alphabetic index entries
24 entriesTerms in the official ICD-10-CM index that lead to D61.01.
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › aplastic › red cell (pure) › congenital
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › Diamond-Blackfan (congenital hypoplastic)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hypoplasia, red blood cells › congenital or familial
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hypoplastic (idiopathic) › congenital or familial (of childhood)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › Joseph-Diamond-Blackfan (congenital hypoplastic)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › pure red cell › congenital
- Aplasia › bone marrow (myeloid) › congenital
- Aplasia › congenital pure red cell
- Aplasia › erythrocyte congenital
- Aplasia › red cell (with thymoma) › congenital
- Aplasia › red cell (with thymoma) › constitutional
- Aplasia › red cell (with thymoma) › hereditary
- Aplasia › red cell (with thymoma) › of infants
- Aplasia › red cell (with thymoma) › primary
- Aplasia › red cell (with thymoma) › pure
- Blackfan-Diamond anemia or syndrome (congenital hypoplastic anemia)
- Diamond-Blackfan anemia (congenital hypoplastic)
- Erythroblastopenia › congenital
- Hypoplasia, hypoplastic › erythroid, congenital
- Joseph-Diamond-Blackfan anemia (congenital hypoplastic)
- Kaznelson's syndrome (congenital hypoplastic anemia)
- Syndrome › Blackfan-Diamond
- Syndrome › Diamond-Blackfan
- Syndrome › Joseph-Diamond-Blackfan
Codes whose notes reference D61.01
MS-DRG v44.0 grouping
All DRGs →Inpatient MS-DRGs this diagnosis can group to, as the principal or a secondary diagnosis, depending on the rest of the claim.
MDC 16 · Diseases and Disorders of the Blood and Blood Forming Organs and Immunological Disorders
- 808Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCCRW 2.1705
- 809Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CCRW 1.2262
- 810Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCCRW 1.075
ICD-9-CM equivalent
Converter →- 284.01Constitutional red blood cell aplasiaexact
From the CMS 2018 General Equivalence Mappings (GEMs), the final GEMs release.
Code history
- 2016
- 2017
- 2018
- 2019
- 2020
- 2021
- 2022
- 2023
- 2024
- 2025
- 2026
- 2027
- FY2016 (effective 10/1/2015): Added (first year of ICD-10-CM)
- No changes since FY2016.
Common questions about D61.01
Is D61.01 billable?
- Yes. D61.01 is a billable/specific ICD-10-CM code valid for FY2027 (October 1, 2026 – September 30, 2027).
Can D61.01 be used as a principal diagnosis?
- Yes. The Medicare Code Editor doesn't restrict D61.01 as a principal diagnosis.
Is D61.01 a CC or MCC?
- D61.01 is a CC (complication or comorbidity) under MS-DRG v44.0, unless excluded by the principal diagnosis.
What DRG does D61.01 group to?
- D61.01 is used in the MS-DRG v44.0 logic for MS-DRG 808 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCC), MS-DRG 809 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CC) and MS-DRG 810 (Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCC). Which one applies depends on whether it is the principal diagnosis and on the rest of the claim.
What is the ICD-9 code for D61.01?
- The CMS General Equivalence Mappings map D61.01 to ICD-9-CM 284.01.