D69.49 ICD-10-CM Code: Other primary thrombocytopenia
D69.49 maps to CMS-HCC V28 112 (RAF 0.450). Documentation must support MEAT. MEAT criteria · RAF calculator · HCC coding software
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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) / Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
D69.49
Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidanceOther primary thrombocytopenia
Low platelet counts caused by bone marrow problems or other primary disorders not classified elsewhere.

Buddy Insight
Other primary thrombocytopenia captures primary platelet production or survival disorders not classified as ITP, Evans syndrome, or hereditary thrombocytopenia.
CMS-HCC V28
MappedHCC 112
RAF 0.450
CMS-HCC V24
MappedHCC 48
RAF 0.192
ACA/HHS
MappedHCC 75
Varies by metal level
ESRD/PACE
MappedHCC 48
RAF 0.063
RXHCC
N/A—
Not mapped
Code Book Path
Inclusion Terms
Official- Megakaryocytic hypoplasia
- Primary thrombocytopenia NOS
Excludes 2
OfficialICD-10-CM does not list Excludes 2 notes for D69.49 in this effective period.
Related Child Codes
Includes
OfficialICD-10-CM does not list Includes notes for D69.49 in this effective period.
Excludes 1
Official- transient neonatal thrombocytopenia (P61.0)
- Wiskott-Aldrich syndrome (D82.0)
Code First
OfficialICD-10-CM does not list Code First sequencing instructions for D69.49 in this effective period.
Use Additional
OfficialICD-10-CM does not list Use Additional Code instructions for D69.49 in this effective period.
Code Also
OfficialICD-10-CM does not list Code Also instructions for D69.49 in this effective period.
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 D69.49 an HCC code?
Yes. D69.49 (Other primary thrombocytopenia) maps to Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions under the CMS-HCC V28 risk adjustment model (and Coagulation Defects and Other Specified Hematological Disorders under V24), with a community non-dual aged RAF of 0.450. It is billable for payment year 2026.
Coder answer: D69.49 is billable and maps to V28 HCC 112, Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions. Open it in the Code Book for the tabular path, RAF, and MEAT checklist.
- Code
- D69.49
- Description
- Other primary thrombocytopenia
- HCC (V28)
- HCC 112 — Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions
- RAF
- 0.450
- Billable
- Yes
- Payment year
- 2026
HCC Category Mapping
Each model's RAF is its CMS base weight for that model's standard population, so 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 segment, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains in use during the transition and for historical data.
Work D69.49 in the Code Book — tabular path, V28 RAF, and MEAT checklist →
MEAT Criteria for D69.49
For D69.49 to count as a valid HCC diagnosis in a given encounter, the provider's documentation must show MEAT: Monitor, Evaluate, Assess, or Treat. A diagnosis from a prior year does not carry forward automatically, it has to be re-documented and supported each calendar year.
- 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
Only one of M/E/A/T is required to support the code, but the documentation must be specific enough to show that the provider actually addressed D69.49 during that encounter, not just copy-forwarded from a problem list.
Coder workflow notes
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What This Code Means
D69.49 is the ICD-10-CM diagnosis code for other primary thrombocytopenia. Low platelet counts caused by bone marrow problems or other primary disorders not classified elsewhere. D69.49 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 coagulation defects, purpura and other hemorrhagic conditions (d65-d69).
Under the CMS-HCC V28 risk adjustment model, D69.49 maps to Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions (HCC 112) with a community, non-dual, aged base RAF weight of 0.450. Under the older CMS-HCC V24 model, D69.49 maps to Coagulation Defects and Other Specified Hematological Disorders (HCC 48) with a community, non-dual, aged base RAF weight of 0.192. V28 is the CMS-HCC risk adjustment model that reached 100% phase-in for payment year 2026, replacing V24 which was used during the PY2024–PY2025 transition.
Rule out secondary causes (medications, infections, splenomegaly) before assigning this code. Because D69.49 maps to a payment HCC, the provider's documentation must satisfy MEAT criteria (Monitor, Evaluate, Assess, or Treat) for the encounter to count toward the patient's Medicare Advantage risk adjustment score. 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, RAF weights, and MEAT documentation criteria for D69.49 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.
Coding Tips
- •Rule out secondary causes (medications, infections, splenomegaly) before assigning this code
- •Document the underlying mechanism if known (decreased production vs. increased destruction)
Clinical Significance
Other primary thrombocytopenia captures primary platelet production or survival disorders not classified as ITP, Evans syndrome, or hereditary thrombocytopenia. This includes conditions such as cyclic thrombocytopenia, amegakaryocytic thrombocytopenia, and other rare primary platelet disorders. It represents a diagnostically challenging category requiring hematology evaluation.
Documentation Requirements
- ✓Document the specific clinical features and laboratory findings differentiating this from ITP and inherited thrombocytopenias.
- ✓Record bone marrow biopsy results if performed (showing megakaryocyte number and morphology), serial platelet counts demonstrating the pattern, and exclusion of secondary causes.
- ✓Note the treatment approach and response.

