C92.12 ICD-10-CM Code: Chronic myeloid leukemia, BCR/ABL-positive, in relapse
C92.12 maps to CMS-HCC V28 22. A source-labeled RAF reference is available. Confirm the documented diagnosis and applicable coding requirements. MEAT criteria · RAF Calculator · HCC coding software
HCC Buddy Code Card
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FY 2026 Apr update / Neoplasms (C00-D49) / Malignant neoplasms of lymphoid, hematopoietic and related tissue (C81-C96)
C92.12
Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidanceChronic myeloid leukemia, BCR/ABL-positive, in relapse
A type of blood cancer (chronic myeloid leukemia) with a specific genetic mutation that has returned after initial treatment.

Buddy Insight
Chronic myeloid leukemia, BCR/ABL-positive, in relapse indicates loss of previously achieved treatment response, which may manifest as hematologic, cytogenetic, or molecular relapse.
CMS-HCC V28
MappedHCC 22
Coefficient HCC 22: 0.363 (Community Non-Dual Aged (CNA))
CMS-HCC V24
HistoricalHistorical
Not used for CY2026 payment
ACA/HHS
MappedHCC 009
Code-level coefficient reference
ESRD/PACE
MappedHCC 9
Code-level coefficient reference
RXHCC
MappedHCC 15
Code-level coefficient reference
Code Book Path
Inclusion Terms
Official- Chronic myelogenous leukemia, Philadelphia chromosome (Ph1) positiveInherited from C92.1
- Chronic myelogenous leukemia, t(9;22) (q34;q11)Inherited from C92.1
- Chronic myelogenous leukemia with crisis of blast cellsInherited from C92.1
Excludes 2
Official- Kaposi's sarcoma of lymph nodes (C46.3)Inherited from C81-C96
- secondary and unspecified neoplasm of lymph nodes (C77.-)Inherited from C81-C96
- secondary neoplasm of bone marrow (C79.52)Inherited from C81-C96
- secondary neoplasm of spleen (C78.89)Inherited from C81-C96
Related Codes
Includes
Official- granulocytic leukemiaInherited from C92
- myelogenous leukemiaInherited from C92
Excludes 1
Official- personal history of leukemia (Z85.6)Inherited from C92, C92.1
- atypical chronic myeloid leukemia BCR/ABL-negative (C92.2-)Inherited from C92, C92.1
- chronic myelomonocytic leukemia (C93.1-)Inherited from C92, C92.1
- chronic myeloproliferative disease (D47.1)Inherited from C92, C92.1
Code First
OfficialNo Code First sequencing instructions are included in this display for C92.12. Check the code and parent instructions in the Code Book.
Use Additional
OfficialNo Use Additional Code instructions are included in this display for C92.12. Check the code and parent instructions in the Code Book.
Code Also
Official- , if applicable, pancytopenia (acquired) (D61.818)Inherited from C92
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 C92.12 an HCC code?
Yes. C92.12 (Chronic myeloid leukemia, BCR/ABL-positive, in relapse) maps to HCC 22, Bladder, Colorectal, and Other Cancers under the CMS-HCC V28 risk adjustment model, with a source-labeled community non-dual aged reference coefficient of 0.363. 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: C92.12 is billable and maps to V28 HCC 22, Bladder, Colorectal, and Other Cancers. Open it in the Code Book for the tabular path, RAF, and MEAT checklist.
- Code
- C92.12
- Description
- Chronic myeloid leukemia, BCR/ABL-positive, in relapse
- HCC (V28)
- HCC 22 — Bladder, Colorectal, and Other Cancers
- RAF reference coefficient
- 0.363
- 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 C92.12 in the Code Book — tabular path, V28 RAF reference, and MEAT checklist →
MEAT review for C92.12
For C92.12, 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
C92.12 is the ICD-10-CM diagnosis code for chronic myeloid leukemia, bcr/abl-positive, in relapse. A type of blood cancer (chronic myeloid leukemia) with a specific genetic mutation that has returned after initial treatment. C92.12 sits in the ICD-10-CM chapter for neoplasms (c00-d49), within the section covering malignant neoplasms of lymphoid, hematopoietic and related tissue (c81-c96).
Under the CMS-HCC V28 risk adjustment model, C92.12 maps to Bladder, Colorectal, and Other Cancers (HCC 22) with a source-labeled community, non-dual, aged reference coefficient of 0.363. No V24 mapping is shown for C92.12; use the applicable model and payment year when reviewing the V28 mapping. 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.
Verify BCR/ABL positivity is documented in the pathology report before assigning this code. For C92.12, 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 C92.12 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.
Coding Tips
- •Verify BCR/ABL positivity is documented in the pathology report before assigning this code
- •Ensure relapse status is clearly documented; do not assume relapse without explicit physician documentation
Clinical Significance
Chronic myeloid leukemia, BCR/ABL-positive, in relapse indicates loss of previously achieved treatment response, which may manifest as hematologic, cytogenetic, or molecular relapse. CML relapse while on TKI therapy may indicate development of resistance mutations (e.g., T315I) and often requires switching to an alternative TKI or consideration of allogeneic transplant. Relapse after TKI discontinuation during treatment-free remission is also captured by this code.
Documentation Requirements
- ✓Documentation must confirm prior remission and evidence of relapse, including rising BCR-ABL1 transcript levels, loss of cytogenetic response, or hematologic recurrence.
- ✓BCR-ABL1 kinase domain mutation testing should be documented at relapse to guide TKI selection.
- ✓Current disease phase (chronic, accelerated, blast crisis) must be specified, as some relapses present with disease acceleration.

