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G71.01

Billable

Duchenne or Becker muscular dystrophy

HCC Category Mapping

V28HCC 197Muscular Dystrophy
0.000
V24HCC 76Muscular Dystrophy
0.358
ESRDHCC 76Muscular Dystrophy
0.000

What This Code Means

A severe inherited muscle disease causing progressive weakness and wasting, with Duchenne type being more severe and Becker type being milder.

Coding Tips

  • Specify whether Duchenne or Becker type when documentation permits; these have different severity and prognosis
  • Document age of onset and progression pattern to support the diagnosis

Clinical Significance

Duchenne or Becker muscular dystrophy are X-linked recessive dystrophinopathies representing the most common and among the most severe forms of muscular dystrophy. Duchenne type has childhood onset with loss of ambulation by adolescence and life-threatening cardiac and respiratory complications. Accurate coding is critical for capturing the extraordinary care complexity including corticosteroids, cardiac monitoring, respiratory support, and mobility aids.

Documentation Requirements

  • Genetic testing confirming dystrophin gene mutation or muscle biopsy showing absent/reduced dystrophin
  • Specification of Duchenne versus Becker type when possible (Duchenne has absent dystrophin, Becker has reduced)
  • Age of onset and progression timeline
  • Current functional status: ambulatory versus non-ambulatory, respiratory function
  • Cardiac evaluation: echocardiogram results, cardiac involvement
  • Current treatment: corticosteroids, cardiac medications, respiratory support

Commonly Confused Codes

Code Hierarchy

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