G71.034 ICD-10-CM Code: Limb girdle muscular dystrophy due to sarcoglycan dysfunction
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
- 3 Excludes2
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.
Most relevant related codes MedCoder-derived
Read off the official notes above and this code’s own position in the tabular list. Which to report is a documentation question; Compare shows the two side by side.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for G71.034 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 G71.034 itself; “inherited from” names the category or block whose note applies here.
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- arthrogryposis multiplex congenita (Q74.3) Compare G71.034 vs Q74.3 →
- metabolic disorders (E70-E88) Compare G71.034 vs E70 →
- myositis (M60.-) Compare G71.034 vs M60 →
Source: inherited from G71
Coder workflow for G71.034
MedCoder structured workflow — derived from this code’s own official record
Before you code G71.034
- G71.034 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).
ReviewG71.0340, G71.0341, G71.0342, G71.0349
See the relationships section · Guide: How to choose an ICD-10-CM code →
- G71.034’s title joins a condition with an associated condition or complication. Confirm each component is documented. Where the classification presumes the link through the “with” convention, only a provider statement that the conditions are unrelated defeats it. A combination code is assigned only when it fully identifies the documented conditions; a required second code for the stage, type or manifestation is still reported when the notes ask for it (Guidelines I.B.9, I.A.15).
Choose the right path
- Does the documentation support one of the more specific codes beneath G71.034?
Yes → Select that code and continue the checks below on its own page.
No → G71.034 cannot be reported as written; query for the specificity its subcategory needs.
Consider G71.034. 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).
- The associated condition or complication
- Whether the associated condition the title names is documented; the “with” convention presumes some links, and a provider statement that the conditions are unrelated defeats it (Guidelines I.A.15).
Official instructions as workflow
Excludes2 — not part of G71.034(3 notes)
Coding workflow: The conditions named in this note are not included in G71.034. 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
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Only one of the components this code’s title joins is documented.
Coding question: Is G71.034 supported?
Path: Review the code for the documented component on its own.
Reason: A combination code is assigned only when it fully identifies the documented conditions; otherwise the documented component takes its own code (Guidelines I.B.9).
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
Guidelines, coding notes, decision aids, relationships (with MS-DRG and CCSR classification), hierarchy, HCC, coverage and the context map: what a coder reaches for after the core. 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 G71.034 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 5 Excludes2 notes: M60 — Myositis (via G71.-), M60-M63 — Disorders of muscles (M60-M63) (via G71.-), M61 — Calcification and ossification of muscle (via G71.-), M62 — Other disorders of muscle (via G71.-), M63 — Disorders of muscle in diseases classified elsewhere (via G71.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 2 Code First instructions across 2 chapters: M62.84 — Sarcopenia (via G71.-), Z99.3 — Dependence on wheelchair (via G71.0.-).
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.
Contextual Map
Every relationship of G71.034 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 G71.034 with these 7 related codes in Claim Check
Hierarchy
- G00-G99 — Chapter 6: Diseases of the Nervous System (G00-G99) (G00-G99)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G70-G73 — Diseases of myoneural junction and muscle[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Referenced by Excludes2 notes
- M60 — Myositis[Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- M60-M63 — Disorders of muscles (M60-M63)[Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- M61 — Calcification and ossification of muscle[Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- M62 — Other disorders of muscle[Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- M63 — Disorders of muscle in diseases classified elsewhere[Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Code First instructions
- M62.84 — Sarcopenia[Code First](via G71.-): “primary disorders of muscles (G71.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Z99.3 — Dependence on wheelchair[Code First](via G71.0.-): “muscular dystrophy (G71.0-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Nearest codes (34)
- G71 — Primary disorders of muscles[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G71.0 — Muscular dystrophy[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G71.00 — Muscular dystrophy, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G71.01 — Duchenne or Becker muscular dystrophy[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G71.02 — Facioscapulohumeral muscular dystrophy[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G71.03 — Limb girdle muscular dystrophies[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G71.031 — Autosomal dominant limb girdle muscular dystrophy[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- G71.032 — Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 26 more
Change history
- FY2023 — Added to the code set[Change history]— CMS release files (code change ledger) · icd10cm-fy2023
Reference
Index terms and tables, 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 G71.034 be billed directly?
No. G71.034 (Limb girdle muscular dystrophy due to sarcoglycan dysfunction) 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. "G71.034 — Limb girdle muscular dystrophy due to sarcoglycan dysfunction." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/g71.034-limb-girdle-muscular-dystrophy-due-to-sarcoglycan-dysfunction
Change history
- FY2023 — October 1, 2022Added to the code setLimb girdle muscular dystrophy due to sarcoglycan dysfunctionFY2023 changes
Nearest Codes in This Family
Official ICD-10-CM classifications closest to G71.034 in its code family, with their registry titles.
- G71.02 — Facioscapulohumeral muscular dystrophy
- G71.03 — Limb girdle muscular dystrophies
- G71.031 — Autosomal dominant limb girdle muscular dystrophy
- G71.032 — Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- G71.033 — Limb girdle muscular dystrophy due to dysferlin dysfunction
- G71.0340 — Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
- G71.0341 — Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- G71.0342 — Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- G71.0349 — Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- G71.035 — Limb girdle muscular dystrophy due to anoctamin-5 dysfunction