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G71.039 ICD-10-CM Code: Limb girdle muscular dystrophy, unspecified

Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.

Coding at a Glance

Tabular directives
3 Excludes2
Risk adjustment
CMS-HCC V28: 1 category · CMS-HCC V22 category 76

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 091 — OTHER DISORDERS OF NERVOUS SYSTEM WITH MCC (MDC 01)
  • MS-DRG 092 — OTHER DISORDERS OF NERVOUS SYSTEM WITH CC (MDC 01)
  • MS-DRG 093 — OTHER DISORDERS OF NERVOUS SYSTEM WITHOUT CC/MCC (MDC 01)

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 197 — Muscular Dystrophy

Other models: CMS-HCC V22 HCC 76

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 G71.039 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 G71.039 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.

Source: inherited from G71

Coder workflow for G71.039

MedCoder structured workflow — derived from this code’s own official record

Before you code G71.039

  1. Unspecified does not mean incorrect. When the record gives no greater specificity, G71.039 may be the appropriate code. Check the record for detail that supports a more specific sibling. An unspecified code is for records that do not provide the detail a more specific code needs; a query, not an assumption, is the route to specificity (Guidelines I.A.9.b, I.B.18).

    ReviewG71.031, G71.032, G71.033, G71.034, G71.035, G71.036, G71.038

    See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →

Choose the right path

  1. Does the record document the detail a more specific sibling code needs?
    Yes → Review the specific siblings in this subcategory.
    No → Continue — G71.039 is appropriate when the documentation goes no further.

    ReviewG71.031, G71.032, G71.033, G71.034, G71.035, G71.036, G71.038

Consider G71.039. 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).
Any detail beyond this code’s title
What the record states that a more specific sibling code would capture — or its absence, which itself supports the unspecified code.

Official instructions as workflow

  • Excludes2 — not part of G71.039(3 notes)

    Coding workflow: The conditions named in this note are not included in G71.039. When the record documents both, both may be reported; the note is a boundary, not a prohibition.

    CompareQ74.3, M60

    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: The provider documents the condition in the terms of this code’s title and records no further detail.

Coding question: Is a more specific sibling code supportable?

Path: Review the specific siblings in this subcategory and what each requires the record to state.

Reason: A more specific code needs documentation of the distinguishing element; without it the unspecified code is appropriate, and a provider query is the route to specificity (Guidelines I.A.9.b, I.B.18).

ReviewG71.031, G71.032, G71.033, G71.034, G71.035, G71.036, G71.038

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

Limb girdle muscular dystrophy, unspecified is a billable ICD-10-CM diagnosis code (G71.039).

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.

Verify Before Coding

  • No Medicare Code Editor or MS-DRG Definitions Manual restrictions apply to this code.

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 G71.039 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.

MS-DRG Grouper Relationships (FY2026)

Potential MS-DRG participation — not a DRG assignment.

FY2026 MS-DRG: not on the CMS CC/MCC list — as a secondary diagnosis this code does not change MS-DRG severity for that release.

Named in the grouper logic of 3 MS-DRGs: DRG 091 (MDC 01), DRG 092 (MDC 01), DRG 093 (MDC 01).

From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.

Clinical classification (AHRQ CCSR):NVS018 — Myopathies (default).

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 CMS-HCC risk category (V28)

CMS maps these diagnoses to the same Hierarchical Condition Category (Muscular Dystrophy) for risk-adjusted payment.

G71.00 — Muscular dystrophy, unspecified, G71.01 — Duchenne or Becker muscular dystrophy, G71.02 — Facioscapulohumeral muscular dystrophy, 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, G71.036 — Limb girdle muscular dystrophy due to fukutin related protein dysfunction, G71.038 — Other limb girdle muscular dystrophy, G71.09 — Other specified muscular dystrophies, G71.11 — Myotonic muscular dystrophy, G71.20 — Congenital myopathy, unspecified, G71.21 — Nemaline myopathy, G71.220 — X-linked myotubular myopathy, G71.228 — Other centronuclear myopathy, G71.29 — Other congenital myopathy

Same clinical category (CCSR)

AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Myopathies).

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, G71.036 — Limb girdle muscular dystrophy due to fukutin related protein dysfunction, G71.038 — Other limb girdle muscular dystrophy, G71.09 — Other specified muscular dystrophies, G71.11 — Myotonic muscular dystrophy, G71.12 — Myotonia congenita, G71.13 — Myotonic chondrodystrophy, G71.14 — Drug induced myotonia, G71.19 — Other specified myotonic disorders, G71.2 — Congenital myopathies, G71.20 — Congenital myopathy, unspecified, G71.21 — Nemaline myopathy, G71.220 — X-linked myotubular myopathy, +53 more

Same Index main term, other category

The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Dystrophy, dystrophia”; these codes share that main term but sit in a different category of the Tabular List.

E23.6 — Other disorders of pituitary gland (adiposogenital), E31.8 — Other polyglandular dysfunction (polyglandular), E45 — Retarded development following protein-calorie malnutrition (nutritional), E72.03 — Lowe's syndrome (oculocerebrorenal), E75.6 — Lipid storage disorder, unspecified (retinal, in, systemic lipidoses), G31.89 — Other specified degenerative diseases of nervous system (infantile neuraxonal), G60.0 — Hereditary motor and sensory neuropathy (muscular, progressive, Charcot-Marietype), G90.2 — Horner's syndrome (cervical sympathetic), H18.50 — Unspecified hereditary corneal dystrophies (cornea), H18.51 — Endothelial corneal dystrophy (Fuchs'), H18.52 — Epithelial (juvenile) corneal dystrophy (cornea, epithelial), H18.53 — Granular corneal dystrophy (cornea, granular), H18.54 — Lattice corneal dystrophy (cornea, lattice), H18.55 — Macular corneal dystrophy (cornea, macular), H18.59 — Other hereditary corneal dystrophies (cornea, specified type NEC), H31.20 — Hereditary choroidal dystrophy, unspecified (choroid), H31.21 — Choroideremia (choroid, choroideremia), H31.22 — Choroidal dystrophy (central areolar) (generalized) (peripapillary) (choroid, central areolar), H31.23 — Gyrate atrophy, choroid (choroid, gyrate atrophy), H31.29 — Other hereditary choroidal dystrophy (choroid, specified type NEC), +12 more

Contextual Map

Every relationship of G71.039 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 G71.039 with these 7 related codes in Claim Check

Hierarchy

Referenced by Excludes2 notes

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-fy2026
  • Z99.3 — Dependence on wheelchair[Code First](via G71.0.-): “muscular dystrophy (G71.0-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026

Clinical classification (CCSR)

Risk adjustment (CMS-HCC)

  • HCC 197 — Muscular Dystrophy [CMS-HCC]— CMS-HCC V28 · 2026

MS-DRG Grouper

MDC crossing

  • MDC 01 — Diseases and Disorders of the Nervous System[MDC crossing]: “Diseases and Disorders of the Nervous System — 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. 8,892 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026

Index entries

  • Dystrophy, dystrophia, Leyden-Möbius[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
  • Dystrophy, dystrophia, Leyden-Möbius, meaning Limb girdle muscular dystrophy NOS[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
  • Dystrophy, dystrophia, muscular, limb-girdle[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026

Nearest codes (34)

Change history

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
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. "G71.039 — Limb girdle muscular dystrophy, unspecified." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/g71.039-limb-girdle-muscular-dystrophy-unspecified

Change history

  • FY2023 — October 1, 2022
    Added to the code set
    Limb girdle muscular dystrophy, unspecified
    FY2023 changes

Nearest Codes in This Family

Official ICD-10-CM classifications closest to G71.039 in its code family, with their registry titles.

View all codes in the G71 family