2027 ICD-10-CM Diagnosis Code C92.A1Acute myeloid leukemia with multilineage dysplasia, in remission
ICD-10-CM Codes›C00–D49›C81-C96›C92
- Billable — Valid for Submission
- CC — Complication or Comorbidity
- Risk Adjusts — HCC 17
- Chronic Condition
C92.A1 is a billable ICD-10-CM diagnosis code for acute myeloid leukemia with multilineage dysplasia, in remission. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 820 through 822, 834 through 839, 850. 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 113 closely related codes. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Leukemia in remission.
For Medicare Advantage risk adjustment, C92.A1 maps to CMS-HCC Category 17 (Cancer Metastatic to Lung, Liver, Brain, and Other Organs; Acute Myeloid Leukemia Except Promyelocytic) under the V28 model, adding a risk factor of about 4.209 for a community, non-dual, aged beneficiary in payment year 2027.
Code Identity
Code Classification
Medicare Risk Adjustment (HCC)Billing
C92.A1 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.
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to C92.A1: its own notes plus those printed at C92, block C81-C96, and Chapter 2. A note printed at a category, block or chapter applies to every code under it.
Includes
Further defines, or gives examples of, the content of the category.
- granulocytic leukemia
- myelogenous leukemia
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
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.
Code Also
A second code may be needed to fully describe the condition; the note gives no sequencing direction.
Notes
General instructions on how these codes are used.
- Functional activity
- All neoplasms are classified in this chapter, whether they are functionally active or not. An additional code from Chapter 4 may be used, to identify functional activity associated with any neoplasm.
- Morphology [Histology]
- Chapter 2 classifies neoplasms primarily by site (topography), with broad groupings for behavior, malignant, in situ, benign, etc. The Table of Neoplasms should be used to identify the correct topography code. In a few cases, such as for malignant melanoma and certain neuroendocrine tumors, the morphology (histologic type) is included in the category and codes.
- Primary malignant neoplasms overlapping site boundaries
- A primary malignant neoplasm that overlaps two or more contiguous (next to each other) sites should be classified to the subcategory/code .8 ('overlapping lesion'), unless the combination is specifically indexed elsewhere. For multiple neoplasms of the same site that are not contiguous, such as tumors in different quadrants of the same breast, codes for each site should be assigned.
- Malignant neoplasm of ectopic tissue
- Malignant neoplasms of ectopic tissue are to be coded to the site mentioned, e.g., ectopic pancreatic malignant neoplasms are coded to pancreas, unspecified (C25.9).
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Referenced in Other NotesGuidance
Instructional notes printed at other codes that name C92.A1, its category, or a range that includes it.
Applicable To 2
These notes mention C92.A1.
Excludes1 4
These codes carry an Excludes1 note naming C92.A1: they are not reported together with it, unless the two conditions are unrelated.
Code First 3
These codes say to code first a condition named in the note, and C92.A1 is one of the conditions named.
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Acute Myeloid Leukemia with Multilineage Dysplasia in Remission
a finding of acute myeloid leukemia with multilineage dysplasia that is not growing and responds to treatment.Leukemia, Myeloid
form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (myeloid progenitor cells) in the bone marrow and other sites.
Patient EducationClinical
Acute Myeloid Leukemia
Leukemia is a term for cancers of the blood cells. Leukemia starts in blood-forming tissues such as the bone marrow. Your bone marrow makes the cells which will develop into white blood cells, red blood cells, and platelets. Each type of cell has a different job:
The full article covers:
- What is leukemia?
- What is acute myeloid leukemia (AML)?
- What causes acute myeloid leukemia (AML)?
- Who is at risk for acute myeloid leukemia (AML)?
- What are the symptoms of acute myeloid leukemia (AML)?
- How is acute myeloid leukemia (AML) diagnosed?
- What are the treatments for acute myeloid leukemia (AML)?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert C92.A1 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About C92.A1Overview
What is the ICD-10 code for acute myeloid leukemia with multilineage dysplasia, in remission?
The ICD-10-CM code for acute myeloid leukemia with multilineage dysplasia, in remission is C92.A1 (sometimes written as C92A1). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
Is C92.A1 (Acute myeloid leukemia with multilineage dysplasia) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report acute myeloid leukemia with multilineage dysplasia, in remission on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does C92.A1 group to?
When acute myeloid leukemia with multilineage dysplasia, in remission is the principal diagnosis on an inpatient stay, it groups to MS-DRG 834, 837, 821, 822, 836, 839, 838, 850, 835, 820, with relative weights from 1.1267 to 8.4076 depending on complications. Higher weights mean higher Medicare reimbursement.
Is C92.A1 a CC or MCC?
CMS lists C92.A1 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 113 closely related codes in its exclusion list.
Can C92.A1 be reported with Z85.6?
Not as a rule. The Excludes1 note at C92, which applies to C92.A1, lists "personal history of leukemia (Z85.6)". 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 C92.A1?
C92.A1 (acute myeloid leukemia with multilineage dysplasia, in remission) maps to CMS-HCC Category 17 (Cancer Metastatic to Lung, Liver, Brain, and Other Organs; Acute Myeloid Leukemia Except Promyelocytic), commonly written as HCC 17, in the CMS-HCC V28 model used for Medicare Advantage risk adjustment in payment year 2027. It mapped to HCC 8 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 19.
Does C92.A1 risk-adjust for Medicare Advantage payment?
Yes. When documented and reported on a Medicare Advantage encounter, C92.A1 adds a risk adjustment factor of about 4.209 to the beneficiary's RAF score for a community, non-dual, aged enrollee (published V28 weights range from 1.952 to 4.235 depending on the payment segment). HCC 17 sits at the top of its hierarchy, so no other condition category supersedes it. See the full factor table on the HCC 17 category page.
