G71.22 ICD-10-CM Code: Centronuclear myopathy
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Official Registry Overview & Definition
Official Tabular Instructional Notes
Sequencing, inclusion, and exclusion notes published for G71.22 in the official ICD-10-CM tabular list.
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 G71.22 vs Q74.3 →
- metabolic disorders (E70-E88) Compare G71.22 vs E70 →
- myositis (M60.-) Compare G71.22 vs M60 →
Frequently Compared Codes
The official Excludes notes on G71.22 name these codes. Each comparison page covers when the two can — or must not — be reported together.
Change history
- FY2021 — 2020-10-01Added to the code setCentronuclear myopathyFY2021 changes
Verify Before Coding
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim.
Contextual Map
Every relationship of G71.22 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.
Hierarchy
- G00-G99 — Chapter 6: Diseases of the Nervous System (G00-G99) (G00-G99) [Hierarchy]
Referenced by Excludes2 notes
- M60 — Myositis [Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)” · check together
- M60-M63 — Disorders of muscles (M60-M63) [Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)” · check together
- M61 — Calcification and ossification of muscle [Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)” · check together
- M62 — Other disorders of muscle [Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)” · check together
- M63 — Disorders of muscle in diseases classified elsewhere [Excludes2](via G71.-): “muscular dystrophies and myopathies (G71-G72)” · check together
Referenced by Code First instructions
- M62.84 — Sarcopenia [Code First](via G71.-): “primary disorders of muscles (G71.-)” · check together
Nearest codes (34)
- G71 — Primary disorders of muscles [Sibling]
- G71.0 — Muscular dystrophy [Sibling]
- G71.00 — Muscular dystrophy, unspecified [Sibling]
- G71.01 — Duchenne or Becker muscular dystrophy [Sibling]
- G71.02 — Facioscapulohumeral muscular dystrophy [Sibling]
- G71.03 — Limb girdle muscular dystrophies [Sibling]
- G71.031 — Autosomal dominant limb girdle muscular dystrophy [Sibling]
- G71.032 — Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction [Sibling]
- and 26 more
Change history
- FY2021 — Added to the code set [Change history]
Referenced by Other Codes
Official ICD-10-CM tabular notes on other codes that name G71.22 or its code family.
5 Excludes2 notes: M60 (via G71.-), M60-M63 (via G71.-), M61 (via G71.-), M62 (via G71.-), M63 (via G71.-).
1 Code First instructions: M62.84 (via G71.-).
Frequently Asked Questions (FAQ) & Clinical Guidance
Can G71.22 be billed directly?
No. G71.22 (Centronuclear myopathy) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to G71.22 in its code family, with their registry titles.
- 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
- G71.228 — Other centronuclear myopathy
- G71.29 — Other congenital myopathy
- G71.3 — Mitochondrial myopathy, not elsewhere classified
- G71.8 — Other primary disorders of muscles