2027 ICD-10-CM Diagnosis Code D61.01Constitutional (pure) red blood cell aplasia
ICD-10-CM Codes›D50–D89›D60-D64›D61
- Billable — Valid for Submission
- CC — Complication or Comorbidity
- Risk Adjusts — HCC 109
- Chronic Condition
D61.01 is a billable ICD-10-CM diagnosis code for constitutional (pure) red blood cell aplasia. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 808 through 810. As a secondary diagnosis, it counts as a complication or comorbidity (CC) and moves an inpatient stay to a higher severity level within its MS-DRG family. It does not count, however, when the principal diagnosis is one of 98 closely related codes. Coders also document this condition as acute pure red cell aplasia. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Aplastic anemia.
For Medicare Advantage risk adjustment, D61.01 maps to CMS-HCC Category 109 (Acquired Hemolytic, Aplastic, and Sideroblastic Anemias) under the V28 model, adding a risk factor of about 1.144 for a community, non-dual, aged beneficiary in payment year 2027.
Code Identity
Code Classification
Medicare Risk Adjustment (HCC)Billing
D61.01 maps to a payment category in the CMS-HCC model used to risk-adjust Medicare Advantage payments. Weights are the published community factors for payment year 2027.
Source: CMS Payment Year 2027 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Acute pure red cell aplasia
- Congenital hypoplastic anemia
- Constitutional aplastic anemia
- Erythroid hypoplasia of bone marrow
- Finding of bone marrow erythropoiesis
- Hypoplastic anemia
- Pure red cell aplasia
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to D61.01: its own notes plus those printed at D61 and Chapter 3. A note printed at a category, block or chapter applies to every code under it.
Applicable To
Conditions this code is used for: synonyms of the title or, for "other specified" codes, the conditions assigned to it. The list is not exhaustive.
- Blackfan-Diamond syndrome
- Congenital (pure) red cell aplasia
- Familial hypoplastic anemia
- Primary (pure) red cell aplasia
- Red cell (pure) aplasia of infants
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
- acquired red cell aplasia (D60.9)
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
- neutropenia (D70.-)
- 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)
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Referenced in Other NotesGuidance
Instructional notes printed at other codes that name D61.01, its category, or a range that includes it.
Excludes1 3
These codes carry an Excludes1 note naming D61.01: they are not reported together with it, unless the two conditions are unrelated.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
congenital D61.01
hypoplasia, red blood cells D61.9
congenital or familial D61.01
congenital D61.01
Aplasia See Also: Agenesis;
congenital D61.01
congenital pure red cell D61.01
erythrocyte congenital D61.01
congenital D61.01
constitutional D61.01
hereditary D61.01
of infants D61.01
primary D61.01
pure D61.01
Erythroblastopenia See Also: Aplasia, red cell; D60.9
congenital D61.01
Syndrome See Also: Disease;
Blackfan-Diamond D61.01
Diamond-Blackfan D61.01
Joseph-Diamond-Blackfan D61.01
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Anemia, Diamond-Blackfan
a rare congenital hypoplastic anemia that usually presents early in infancy. the disease is characterized by a moderate to severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular bone marrow with erythroid hypoplasia, and an increased risk of developing leukemia. (curr opin hematol 2000 mar;7(2):85-94)
Patient EducationClinical
Anemia
If you have anemia, your blood does not carry enough oxygen to the rest of your body. The most common cause of anemia is not having enough iron. Your body needs iron to make hemoglobin. Hemoglobin is an iron-rich protein that gives the red color to blood. It carries oxygen from the lungs to the rest of the body.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert D61.01 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About D61.01Overview
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 (sometimes written as D6101). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
Is D61.01 (Constitutional aplastic anemia) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report constitutional (pure) red blood cell aplasia on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does D61.01 group to?
When constitutional (pure) red blood cell aplasia is the principal diagnosis on an inpatient stay, it groups to MS-DRG 808, 809, 810, with relative weights from 1.0749 to 2.1706 depending on complications. Higher weights mean higher Medicare reimbursement.
Is D61.01 a CC or MCC?
CMS lists D61.01 as a CC (complication or comorbidity) for FY 2027. Reported as a secondary diagnosis, it moves the inpatient stay to a higher-weighted DRG within its severity family. It does not count when the principal diagnosis is one of the 98 closely related codes in its exclusion list.
Can D61.01 be reported with D60.9?
Not as a rule. The Excludes1 note on D61.01 lists "acquired red cell aplasia (D60.9)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).
What HCC is D61.01?
D61.01 (constitutional (pure) red blood cell aplasia) maps to CMS-HCC Category 109 (Acquired Hemolytic, Aplastic, and Sideroblastic Anemias), commonly written as HCC 109, in the CMS-HCC V28 model used for Medicare Advantage risk adjustment in payment year 2027. It mapped to HCC 46 under the retired V24 model. It also maps in the PACE (CMS-HCC V22), ESRD (V21), and ESRD (V24) models. In the Part D prescription drug model it maps to RxHCC 96.
Does D61.01 risk-adjust for Medicare Advantage payment?
Yes. When documented and reported on a Medicare Advantage encounter, D61.01 adds a risk adjustment factor of about 1.144 to the beneficiary's RAF score for a community, non-dual, aged enrollee (published V28 weights range from 0.529 to 1.815 depending on the payment segment). HCC 109 sits at the top of its hierarchy, so no other condition category supersedes it. See the full factor table on the HCC 109 category page.