M31.1 ICD-10-CM Code: Thrombotic microangiopathy
Compare with another codeCheck this code on a claim
Billing Status: NO. This is a non-billable ICD-10-CM code: report a more specific billable code beneath it.
Coding at a Glance
- Tabular directives
- 4 inclusion terms · 1 Excludes1
Not billable · FY2027A non-billable heading in the tabular list: report a more specific code beneath it.
What you need to know
Source: CMS/NCHS Official ICD-10-CM tabular notes, quoted. From the CMS/NCHS tabular list for the release in force. A note the category or block publishes applies to this code too; the Instructions section marks which is which.
- Excludes1Never report with this code
- autoimmune disease, single organ or single cell-type -code to relevant condition category
- IncludesWhat this code covers
- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for M31.1 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026
Trace:FY2027 changesChange historyRelease, file and checksum
Notes without a marker are published on M31.1 itself; “inherited from” names the category or block whose note applies here.
Includes
Conditions the official ICD-10-CM tabular list includes under this code.
- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
Source: inherited from M30-M36
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).
- autoimmune disease, single organ or single cell-type -code to relevant condition category
Source: inherited from M30-M36
Coder workflow for M31.1
MedCoder structured workflow — derived from this code’s own official record
Before you code M31.1
- M31.1 is not reportable as written. Select the more specific code beneath it that the documentation supports. Codes are reported to the highest level of specificity the classification provides (Guidelines I.B.2).
See the relationships section · Guide: How to choose an ICD-10-CM code →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with M31.1. 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 one of the more specific codes beneath M31.1?
Yes → Select that code and continue the checks below on its own page.
No → M31.1 cannot be reported as written; query for the specificity its subcategory needs. - Does the documentation support a condition named in M31.1’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.
Consider M31.1. Then 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).
Official instructions as workflow
Excludes1 — check before selecting M31.1(1 note)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with M31.1: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
See the official tabular notes · Guidelines I.A.12.a
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition M31.1 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).
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.
Coding context
The comparisons, hierarchy, index entries, guidelines, relationships, risk-adjustment and coverage context a coder commonly needs. Each section names whether it is official source data, a MedCoder-derived relationship or MedCoder editorial.
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.
Verify Before Coding
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-derived relationships — computed from published CMS and AHRQ datasets
Other codes that name M31.1 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: L94 — Other localized connective tissue disorders (via M31.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 2 Excludes2 notes across 2 chapters: I77 — Other disorders of arteries and arterioles (via M31.-), J82 — Pulmonary eosinophilia, not elsewhere classified (via M31.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 1 Code First instruction: J84.170 — Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere (via M31.-).
Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.
Clinical classification (AHRQ CCSR):MUS024 — Systemic lupus erythematosus and connective tissue disorders (default); CIR037 — Vasculitis.
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 category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical categories (Systemic lupus erythematosus and connective tissue disorders, Vasculitis).
M05.271 — Rheumatoid vasculitis with rheumatoid arthritis of right ankle and foot, M05.272 — Rheumatoid vasculitis with rheumatoid arthritis of left ankle and foot, M05.279 — Rheumatoid vasculitis with rheumatoid arthritis of unspecified ankle and foot, M05.29 — Rheumatoid vasculitis with rheumatoid arthritis of multiple sites, M30.0 — Polyarteritis nodosa, M30.1 — Polyarteritis with lung involvement [Churg-Strauss], M30.2 — Juvenile polyarteritis, M30.3 — Mucocutaneous lymph node syndrome [Kawasaki], M30.8 — Other conditions related to polyarteritis nodosa, M31.0 — Hypersensitivity angiitis, M31.10 — Thrombotic microangiopathy, unspecified, M31.11 — Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA], M31.19 — Other thrombotic microangiopathy, M31.2 — Lethal midline granuloma, M31.30 — Wegener's granulomatosis without renal involvement, M31.31 — Wegener's granulomatosis with renal involvement, M31.4 — Aortic arch syndrome [Takayasu], M31.5 — Giant cell arteritis with polymyalgia rheumatica, M31.6 — Other giant cell arteritis, M31.7 — Microscopic polyangiitis, +101 more
Contextual Map
Every relationship of M31.1 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 M31.1 with these 4 related codes in Claim Check
Hierarchy
- M00-M99 — Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (M00-M99) (M00-M99)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M30-M36 — Systemic connective tissue disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Referenced by Excludes1 notes
- L94 — Other localized connective tissue disorders[Excludes1](via M31.-): “systemic connective tissue disorders (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Excludes2 notes
- I77 — Other disorders of arteries and arterioles[Excludes2](via M31.-): “collagen (vascular) diseases (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- J82 — Pulmonary eosinophilia, not elsewhere classified[Excludes2](via M31.-): “pulmonary eosinophilia due to systemic connective tissue disorders (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Code First instructions
- J84.170 — Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere[Code First](via M31.-): “systemic connective tissue disorders (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Clinical classification (CCSR)
- MUS024 — Systemic lupus erythematosus and connective tissue disorders[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
- CIR037 — Vasculitis[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
Nearest codes (15)
- M31 — Other necrotizing vasculopathies[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M31.0 — Hypersensitivity angiitis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M31.10 — Thrombotic microangiopathy, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M31.11 — Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA][Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M31.19 — Other thrombotic microangiopathy[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M31.2 — Lethal midline granuloma[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M31.3 — Wegener's granulomatosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- M31.30 — Wegener's granulomatosis without renal involvement[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 7 more
Change history (2)
- FY2022 — Became a non-billable header[Change history]— CMS release files (code change ledger) · icd10cm-fy2022
- and 1 more
Deep reference
Published questions and FAQ, every source behind this page with its release and checksum, the date-of-service check and the complete change history.
Common coding questions
MedCoder editorial
Can M31.1 be billed directly?
No. M31.1 (Thrombotic microangiopathy) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
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 FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v44.0 (October 2026) 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-derived 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 editorial 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.
Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 20, 2026 · All releases and sources
Labels on this page: Official source data · MedCoder-derived relationship · MedCoder editorial explanation. How to read the labels · All data sources and release dates · CMS coding rules
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. "M31.1 — Thrombotic microangiopathy." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/m31.1-thrombotic-microangiopathy
Change history
- FY2022 — October 1, 2021Became a non-billable headerFY2022 changes
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionThrombotic microangiopathy
Nearest Codes in This Family
Official ICD-10-CM classifications closest to M31.1 in its code family, with their registry titles.
- M31 — Other necrotizing vasculopathies
- M31.0 — Hypersensitivity angiitis
- M31.10 — Thrombotic microangiopathy, unspecified
- M31.11 — Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA]
- M31.19 — Other thrombotic microangiopathy
- M31.2 — Lethal midline granuloma
- M31.3 — Wegener's granulomatosis
- M31.30 — Wegener's granulomatosis without renal involvement
- M31.31 — Wegener's granulomatosis with renal involvement
- M31.4 — Aortic arch syndrome [Takayasu]