D60.0 ICD-10-CM Code: Chronic acquired pure red cell aplasia
D60.0 maps to CMS-HCC V28 109. A source-labeled RAF reference is available. Confirm the documented diagnosis and applicable coding requirements. MEAT criteria · RAF Calculator · HCC Buddy coding tools
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FY 2026 Apr update / Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) / Aplastic and other anemias and other bone marrow failure syndromes (D60-D64)
D60.0
Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidanceChronic acquired pure red cell aplasia
A long-term condition where the bone marrow fails to produce red blood cells while other blood cell production remains normal.

Buddy Insight
Chronic acquired pure red cell aplasia is a rare hematological condition where the bone marrow selectively fails to produce red blood cell precursors while maintaining normal white blood cell and platelet production.
CMS-HCC V28
MappedHCC 109
Coefficient HCC 109: 1.144 (Community Non-Dual Aged (CNA))
CMS-HCC V24
HistoricalHistorical
Not used for CY2026 payment
ACA/HHS
MappedHCC 068
Code-level coefficient reference
ESRD/PACE
MappedHCC 46
Code-level coefficient reference
RXHCC
MappedHCC 96
Code-level coefficient reference
Code Book Path
Inclusion Terms
OfficialNo inclusion terms are included in this display for D60.0. Check the code and parent instructions in the Code Book.
Excludes 2
Official- autoimmune disease (systemic) NOS (M35.9)Inherited from D50-D89
- certain conditions originating in the perinatal period (P00-P96)Inherited from D50-D89
- complications of pregnancy, childbirth and the puerperium (O00-O9A)Inherited from D50-D89
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)Inherited from D50-D89
- endocrine, nutritional and metabolic diseases (E00-E88)Inherited from D50-D89
- human immunodeficiency virus [HIV] disease (B20)Inherited from D50-D89
- injury, poisoning and certain other consequences of external causes (S00-T88)Inherited from D50-D89
- neoplasms (C00-D49)Inherited from D50-D89
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)Inherited from D50-D89
Related Codes
Includes
Official- red cell aplasia (acquired) (adult) (with thymoma)Inherited from D60
Excludes 1
Official- congenital red cell aplasia (D61.01)Inherited from D60
Code First
OfficialNo Code First sequencing instructions are included in this display for D60.0. Check the code and parent instructions in the Code Book.
Use Additional
OfficialNo Use Additional Code instructions are included in this display for D60.0. Check the code and parent instructions in the Code Book.
Code Also
OfficialNo Code Also instructions are included in this display for D60.0. Check the code and parent instructions in the Code Book.
Buddy Documentation Tip
MEAT Support
Audit Caution
Common Mistakes
Current with CMS: FY2026 ICD-10-CM Apr 1 update (effective Apr 1 – Sep 30, 2026) · CMS-HCC V28, 100% phased in for payment year 2026. FY2027 code set already staged for October 1, 2026. How HCC Buddy stays current →
Is D60.0 an HCC code?
Yes. D60.0 (Chronic acquired pure red cell aplasia) maps to HCC 109, Acquired Hemolytic, Aplastic, and Sideroblastic Anemias under the CMS-HCC V28 risk adjustment model, with a source-labeled community non-dual aged reference coefficient of 1.144. Source-labeled code-level coefficients are references, not member totals. Actual contribution depends on complete member context, hierarchy and cleanup rules, interactions, and model year. HCC Buddy's RAF Calculator supports CMS-HCC V28 PY2026 and shows no score unless every required source and calculation check passes. It is billable for payment year 2026.
Coder answer: D60.0 is billable and maps to V28 HCC 109, Acquired Hemolytic, Aplastic, and Sideroblastic Anemias. Open it in the Code Book for the tabular path, RAF, and MEAT checklist.
- Code
- D60.0
- Description
- Chronic acquired pure red cell aplasia
- HCC (V28)
- HCC 109 — Acquired Hemolytic, Aplastic, and Sideroblastic Anemias
- RAF reference coefficient
- 1.144
- Billable
- Yes
- Payment year
- 2026
HCC Category Mapping
These are source-labeled model coefficients, not member totals. A category may still be removed by hierarchy or model cleanup rules. Weights are not directly comparable across models: CMS-HCC V28 and V24 use Community, Non-Dual, Aged; ESRD uses the dialysis continuing-enrollee model; RxHCC is the Part D continuing-enrollee, non-low-income, aged weight (a larger scale than CMS-HCC). ACA/HHS has no single weight — it varies by metal level. Actual per-patient RAF contribution depends on member context, hierarchy and cleanup rules, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains available for historical review.
Work D60.0 in the Code Book — tabular path, V28 RAF reference, and MEAT checklist →
MEAT review for D60.0
For D60.0, confirm that the documentation supports the diagnosis and meets the applicable coding, encounter, program and payer requirements. MEAT (Monitor, Evaluate, Assess, or Treat) is a review mnemonic, not a universal CMS coding rule.
- MMonitor: signs, symptoms, disease progression, or lab trending documented in the note
- EEvaluate: test results, medication response, or physical findings reviewed by the provider
- AAssess: explicit mention in the assessment or plan with acknowledgment of status
- TTreat: medication, referral, procedure, therapy, or counseling tied to the diagnosis
Coder workflow notes
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What This Code Means
D60.0 is the ICD-10-CM diagnosis code for chronic acquired pure red cell aplasia. A long-term condition where the bone marrow fails to produce red blood cells while other blood cell production remains normal. D60.0 sits in the ICD-10-CM chapter for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (d50-d89), within the section covering aplastic and other anemias and other bone marrow failure syndromes (d60-d64).
Under the CMS-HCC V28 risk adjustment model, D60.0 maps to Acquired Hemolytic, Aplastic, and Sideroblastic Anemias (HCC 109) with a source-labeled community, non-dual, aged reference coefficient of 1.144. For CY2026 non-PACE Medicare Advantage, CMS uses 100% of the 2024 CMS-HCC model (V28). PACE uses a separate model blend. Source-labeled code-level coefficients are references, not member totals. Actual contribution depends on complete member context, hierarchy and cleanup rules, interactions, and model year. HCC Buddy's RAF Calculator supports CMS-HCC V28 PY2026 and shows no score unless every required source and calculation check passes.
This code indicates a chronic/persistent condition; document the duration and any treatment responses in the medical record. For D60.0, confirm that the documentation supports the diagnosis and meets the applicable coding, encounter, program and payer requirements. MEAT (Monitor, Evaluate, Assess, or Treat) is a review mnemonic, not a universal CMS coding rule. When documentation is ambiguous, coders should issue a provider query rather than assume the highest-specificity variant.
HCC Buddy maintains structured V28 and V24 mapping, source-labeled coefficient references, and MEAT documentation criteria for D60.0 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.
Coding Tips
- •This code indicates a chronic/persistent condition; document the duration and any treatment responses in the medical record
- •Distinguish from transient forms (D60.1) by confirming the condition has lasted more than a few weeks
Clinical Significance
Chronic acquired pure red cell aplasia is a rare hematological condition where the bone marrow selectively fails to produce red blood cell precursors while maintaining normal white blood cell and platelet production. The chronic designation indicates persistence beyond weeks to months, distinguishing it from transient forms. Common associations include thymoma (up to 50% of cases), autoimmune disorders, lymphoproliferative diseases, and parvovirus B19 persistence in immunocompromised patients. Patients typically present with severe normocytic anemia with absent reticulocytes.
Documentation Requirements
- ✓Document bone marrow biopsy findings showing absent or near-absent erythroid precursors with preserved myeloid and megakaryocytic lineages.
- ✓Record hemoglobin levels, reticulocyte count (characteristically near zero), and normal white blood cell and platelet counts.
- ✓Include workup for underlying causes: computed tomography chest for thymoma, parvovirus B19 testing, autoimmune serologies, and lymphoproliferative disease screening.
- ✓Document treatment response to immunosuppressive therapy, erythropoietin, or thymectomy if applicable.
Commonly Confused Codes
- •D60.1 (Transient acquired pure red cell aplasia) is for temporary episodes resolving within weeks.
- •D60.9 (Acquired pure red cell aplasia, unspecified) does not specify chronicity.
- •D61.01 (Constitutional pure red blood cell aplasia) also known as Diamond-Blackfan anemia is congenital, not acquired.
- •D61.9 (Aplastic anemia, unspecified) involves all cell lines, not isolated red cell failure.

