D89.811 ICD-10-CM Code: Chronic graft-versus-host disease
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v43, Appendix B.
- MS-DRG 808 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC (MDC 16)
- MS-DRG 809 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC (MDC 16)
- MS-DRG 810 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC (MDC 16)
A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.
Risk Adjustment (CMS-HCC)
Payment categories this diagnosis maps to under CMS-HCC V28, payment year 2026.
- HCC 454 — Stem Cell, Including Bone Marrow, Transplant Status/Complications
Other models: CMS-HCC V22 HCC 47 · RxHCC V08 HCC 395
Risk scores depend on the enrollee's full accepted diagnosis set and segment; a category mapping alone does not determine payment.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for D89.811 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on D89.811 itself; “inherited from” names the category or block whose note applies here.
This page already reflects the FY2027 tabular note taking effect October 1, 2026.
Includes
Conditions the official ICD-10-CM tabular list includes under this code.
- defects in the complement system
- immunodeficiency disorders, except human immunodeficiency virus [HIV] disease
- sarcoidosis
Source: inherited from D80-D89
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- hyperglobulinemia NOS (R77.1) inherited from D89Compare D89.811 vs R77.1 →
- monoclonal gammopathy (of undetermined significance) (D47.2) inherited from D89Compare D89.811 vs D47.2 →
- autoimmune disease (systemic) NOS (M35.9) inherited from D80-D89Compare D89.811 vs M35.9 →
- functional disorders of polymorphonuclear neutrophils (D71-) inherited from D80-D89Compare D89.811 vs D71 →
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- transplant failure and rejection (T86.-) inherited from D89Compare D89.811 vs T86 →
- human immunodeficiency virus [HIV] disease (B20) inherited from D80-D89Compare D89.811 vs B20 →
Coder workflow for D89.811
MedCoder structured workflow — derived from this code’s own official record
Before you code D89.811
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with D89.811. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support a condition named in D89.811’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue. - Is the underlying (etiologic) condition the Code First note names documented?
Yes → Sequence the underlying condition first, then D89.811.
No → Continue; do not add an underlying condition the record does not document.
Consider D89.811. Then work the Use Additional Code note, and confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
- Acuity
- Acute or chronic as documented; when both are documented and separate codes exist, both are reported with the acute code first (Guidelines I.B.8).
- The underlying (etiologic) condition
- Named in the Code First note; sequenced before this code when documented (Guidelines I.A.13).
- The conditions the Use Additional Code note names
- Reported with this code when documented; a conditional instruction (“if applicable”, “if known”) applies only when the record supports it.
Official instructions as workflow
Excludes1 — check before selecting D89.811(4 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with D89.811: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareR77.1, D47.2, M35.9, D71
See the official tabular notes · Guidelines I.A.12.a
Excludes2 — not part of D89.811(2 notes)
Coding workflow: The conditions named in this note are not included in D89.811. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
See the official tabular notes · Guidelines I.A.12.b
Code First — sequencing check(3 notes)
Coding workflow: Check whether the underlying or etiologic condition the note names is documented. When it is, sequence it before D89.811. Do not add an underlying condition the record does not document.
See the official tabular notes · Guidelines I.A.13
Use Additional Code — after identifying D89.811(5 notes)
Coding workflow: Check whether the documentation supports the additional code(s) the note names, and report them with D89.811 when it does. Where the instruction is conditional (“if applicable”, “if known”), it applies only when the record documents the condition.
ReviewL30.8, R19.7, R17, L65.9
See the official tabular notes · Guidelines I.A.13
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition D89.811 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
Documentation: The underlying condition the Code First note names is documented alongside this condition.
Coding question: How are the two sequenced?
Path: Review the Code First note.
Reason: The underlying condition is sequenced first and the manifestation follows (Guidelines I.A.13).
Documentation: A condition the Use Additional Code note names is documented.
Coding question: Is a second code reported with D89.811?
Path: Review the Use Additional Code note and the code it names.
Reason: The additional code is reported when the record documents the condition; a conditional instruction applies only when its condition is met (Guidelines I.A.13).
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Indexed Clinical Terms (3)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
Official Coding Guidelines
No excerpt in the ICD-10-CM Official Guidelines names this code specifically. Its chapter carries only this chapter-wide note:
Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
Reserved for future guideline expansion
Decision Points
The directives on this code's own record, as a pre-claim checklist.
- Sequencing: 3 Code First instructions — the underlying condition is sequenced before this code when present. See the Code First notes
- 5 Use Additional Code instructions — report the named additional code(s) when the documentation supports them. See the Use Additional Code notes
- 4 Excludes1 entries — codes named there are generally not reported together with this code (Guidelines I.A.12.a). See the Excludes1 notes
- 2 Excludes2 entries — those conditions are not part of this code and may be reported additionally when documented. See the Excludes2 notes
Checklist rows are derived from this code's own official directives; the wording of each check is MedCoder editorial. The official notes themselves are in the sections each row links to.
Verify Before Coding
- Principal-diagnosis restriction. The Medicare Code Editor lists this code as unacceptable as a principal diagnosis: it describes a circumstance influencing health status rather than a current illness or injury being treated. It is valid as a secondary diagnosis.
- CC as a secondary diagnosis (FY2026). Can raise the stay's MS-DRG severity tier.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
Other codes that name D89.811 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 1 Excludes1 note: D72 — Other disorders of white blood cells (via D89.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 3 Use Additional Code instructions across 2 chapters: M31.11 — Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA] (via D89.81.-), T80.89 — Other complications following infusion, transfusion and therapeutic injection (via D89.81.-), T86 — Complications of transplanted organs and tissue (via D89.81.-).
These codes instruct coders to additionally report this code when it applies.
Referenced by 1 Code Also instruction: J44.81 — Bronchiolitis obliterans and bronchiolitis obliterans syndrome.
These codes suggest coding this condition alongside when both are present.
MS-DRG Grouper Relationships (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 MS-DRG: CC — Complication or Comorbidity. Reported as a secondary diagnosis, this code raises the stay's MS-DRG severity tier — except when the principal diagnosis is one of 45 clinically related codes on its CMS exclusion list.
Named in the grouper logic of 3 MS-DRGs: DRG 808 (MDC 16), DRG 809 (MDC 16), DRG 810 (MDC 16).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):BLD008 — Immunity disorders (default); INJ036 — Complication of transplanted organs or tissue, initial encounter.
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.
Related Codes
Same clinical process (MS-DRG)
Acts as CC — raises the severity of other admissions. CMS groups these diagnoses into one MS-DRG principal-diagnosis exclusion process — a CC/MCC on this list never raises severity when the principal diagnosis is also on it.
D78.81 — Other intraoperative complications of the spleen, D78.89 — Other postprocedural complications of the spleen, E89.810 — Postprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure, E89.811 — Postprocedural hemorrhage of an endocrine system organ or structure following other procedure, E89.820 — Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure, E89.821 — Postprocedural hematoma of an endocrine system organ or structure following other procedure, E89.822 — Postprocedural seroma of an endocrine system organ or structure following an endocrine system procedure, E89.823 — Postprocedural seroma of an endocrine system organ or structure following other procedure, E89.89 — Other postprocedural endocrine and metabolic complications and disorders, H59.011 — Keratopathy (bullous aphakic) following cataract surgery, right eye, H59.012 — Keratopathy (bullous aphakic) following cataract surgery, left eye, H59.013 — Keratopathy (bullous aphakic) following cataract surgery, bilateral, H59.019 — Keratopathy (bullous aphakic) following cataract surgery, unspecified eye, H59.031 — Cystoid macular edema following cataract surgery, right eye, H59.032 — Cystoid macular edema following cataract surgery, left eye, H59.033 — Cystoid macular edema following cataract surgery, bilateral, H59.039 — Cystoid macular edema following cataract surgery, unspecified eye, H59.091 — Other disorders of the right eye following cataract surgery, H59.092 — Other disorders of the left eye following cataract surgery, H59.093 — Other disorders of the eye following cataract surgery, bilateral, +25 more
Principal diagnosis restriction (Medicare Code Editor)
Not acceptable as a principal diagnosis on an inpatient claim.
Same CMS-HCC risk category (V28)
CMS maps these diagnoses to the same Hierarchical Condition Category (Stem Cell, Including Bone Marrow, Transplant Status/Complications) for risk-adjusted payment.
D89.810 — Acute graft-versus-host disease, D89.812 — Acute on chronic graft-versus-host disease, D89.813 — Graft-versus-host disease, unspecified, M31.11 — Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA], T86.00 — Unspecified complication of bone marrow transplant, T86.01 — Bone marrow transplant rejection, T86.02 — Bone marrow transplant failure, T86.03 — Bone marrow transplant infection, T86.09 — Other complications of bone marrow transplant, T86.5 — Complications of stem cell transplant, Z48.290 — Encounter for aftercare following bone marrow transplant, Z94.81 — Bone marrow transplant status, Z94.84 — Stem cells transplant status
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical categories (Immunity disorders, Complication of transplanted organs or tissue, initial encounter).
D89.1 — Cryoglobulinemia, D89.2 — Hypergammaglobulinemia, unspecified, D89.3 — Immune reconstitution syndrome, D89.40 — Mast cell activation, unspecified, D89.41 — Monoclonal mast cell activation syndrome, D89.42 — Idiopathic mast cell activation syndrome, D89.43 — Secondary mast cell activation, D89.44 — Hereditary alpha tryptasemia, D89.49 — Other mast cell activation disorder, D89.810 — Acute graft-versus-host disease, D89.812 — Acute on chronic graft-versus-host disease, D89.813 — Graft-versus-host disease, unspecified, D89.82 — Autoimmune lymphoproliferative syndrome [ALPS], D89.831 — Cytokine release syndrome, grade 1, D89.832 — Cytokine release syndrome, grade 2, D89.833 — Cytokine release syndrome, grade 3, D89.834 — Cytokine release syndrome, grade 4, D89.835 — Cytokine release syndrome, grade 5, D89.839 — Cytokine release syndrome, grade unspecified, D89.84 — IgG4-related disease, +157 more
Contextual Map
Every relationship of D89.811 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run D89.811 with these 5 related codes in Claim Check
Hierarchy
- D50-D89 — Chapter 3: Diseases of the Blood and Blood-forming Organs and Certain Disorders Involving the Immune Mechanism (D50-D89) (D50-D89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D80-D89 — Certain disorders involving the immune mechanism[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Referenced by Excludes1 notes
- D72 — Other disorders of white blood cells[Excludes1](via D89.-): “immunity disorders (D80-D89)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Use Additional Code instructions
- M31.11 — Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA][Use Additional Code](via D89.81.-): “graft versus host disease (D89.81-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- T80.89 — Other complications following infusion, transfusion and therapeutic injection[Use Additional Code](via D89.81.-): “code to identify graft-versus-host reaction, if applicable, (D89.81-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- T86 — Complications of transplanted organs and tissue[Use Additional Code](via D89.81.-): “graft-versus-host disease (D89.81-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Code Also instructions
- J44.81 — Bronchiolitis obliterans and bronchiolitis obliterans syndrome[Code Also]: “chronic graft-versus-host disease (D89.811)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- BLD008 — Immunity disorders[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
- INJ036 — Complication of transplanted organs or tissue, initial encounter[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
Risk adjustment (CMS-HCC)
- HCC 454 — Stem Cell, Including Bone Marrow, Transplant Status/Complications [CMS-HCC]— CMS-HCC V28 · 2026
MS-DRG Grouper
- CC — Complication or Comorbidity [MS-DRG severity]: “As a secondary diagnosis this code can raise the stay's MS-DRG severity tier (CC).”— CMS MS-DRG Definitions Manual (Appendix C) · FY2026
- DRG 808 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC[MS-DRG]: “MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC (MDC 16)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 809 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC[MS-DRG]: “MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC (MDC 16)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 810 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC[MS-DRG]: “MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC (MDC 16)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 16 — Diseases and Disorders of Blood, Blood Forming Organs and Immunologic Disorders[MDC crossing]: “Diseases and Disorders of Blood, Blood Forming Organs and Immunologic Disorders — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 1,614 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries
- Disease, diseased, graft-versus-host (GVH), chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Disease, diseased, host-versus-graft, chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Graft-versus-host disease, chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
Nearest codes (28)
- D89 — Other disorders involving the immune mechanism, not elsewhere classified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D89.0 — Polyclonal hypergammaglobulinemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D89.1 — Cryoglobulinemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D89.2 — Hypergammaglobulinemia, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D89.3 — Immune reconstitution syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D89.4 — Mast cell activation syndrome and related disorders[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D89.40 — Mast cell activation, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D89.41 — Monoclonal mast cell activation syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 20 more
Change history (3)
- FY2027 — Excludes2 note will be added[Change history]— CMS release files (code change ledger) · icd10cm-fy2027
- and 2 more
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Coding guidelines Official source data
- ICD-10-CM Official Guidelines for Coding and Reporting (FY2026), quoted by section Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 2026) Release, file and checksum · Publisher’s page
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v43 Release, file and checksum · Publisher’s page
- Risk adjustment Official source data
- 2026 Mid-Year Final ICD-10 Mappings + Model Software (cms.gov/files/zip/2026-midyear-final-icd-10-mappings.zip, 2026-midyear-final-model-software.zip) — CMS-HCC V28, PY2026 mid-year final release Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "D89.811 — Chronic graft-versus-host disease." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/d89.811-chronic-graft-versus-host-disease
Change history
- Upcoming · effective FY2027 — October 1, 2026Excludes2 note will be addedhuman immunodeficiency virus [HIV] disease (B20)FY2027 changes
- Upcoming · effective FY2027 — October 1, 2026Excludes1 note will be removedhuman immunodeficiency virus [HIV] disease (B20)FY2027 changes
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionChronic graft-versus-host disease
Nearest Codes in This Family
Official ICD-10-CM classifications closest to D89.811 in its code family, with their registry titles.
- D89.44 — Hereditary alpha tryptasemia
- D89.49 — Other mast cell activation disorder
- D89.8 — Other specified disorders involving the immune mechanism, not elsewhere classified
- D89.81 — Graft-versus-host disease
- D89.810 — Acute graft-versus-host disease
- D89.812 — Acute on chronic graft-versus-host disease
- D89.813 — Graft-versus-host disease, unspecified
- D89.82 — Autoimmune lymphoproliferative syndrome [ALPS]
- D89.83 — Cytokine release syndrome
- D89.831 — Cytokine release syndrome, grade 1