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G71.11

Myotonic muscular dystrophy

Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 11 never code together
G71code
Excludes2
  • arthrogryposis multiplex congenita (Q74.3)Q74.3
  • metabolic disorders (E70-E88)E70-E88
  • myositis (M60.-)M60.-
G00-G99chapter
Excludes2
  • certain conditions originating in the perinatal period (P04-P96)P04-P96
  • certain infectious and parasitic diseases (A00-B99)A00-B99
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)Q00-Q99
  • endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
  • injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
  • neoplasms (C00-D49)C00-D49
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94

Excludes2 — not included here, but the patient may have both. Code both when documented.

Instructional notes 5
G71.11code
Inclusion terms
  • Dystrophia myotonica [Steinert]
  • Myotonia atrophica
  • Myotonic dystrophy
  • Proximal myotonic myopathy (PROMM)
  • Steinert disease
Index entries leading here 11
  • Myotonia (acquisita) (intermittens) M62.89
  • Atrophy, atrophic (of)
    • myotonia G71.11
    • muscle, muscular (diffuse) (general) (idiopathic) (primary) M62.50
  • Disease, diseased — see also Syndrome
  • Syndrome — see also Disease
    • Batten-Steinert G71.11
    • Curschmann (-Batten) (-Steinert) G71.11
  • Batten-Steinert syndrome G71.11
  • Cardiomyopathy (familial) (idiopathic) I42.9
    • due to
  • Dystrophy, dystrophia
    • muscular G71.00
      • congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber) G71.09
      • myotonic G71.11
    • myotonic, myotonica G71.11
  • Curschmann (-Batten) (-Steinert) disease or syndrome G71.11
  • Myocardiopathy (congestive) (constrictive) (familial) (hypertrophic nonobstructive) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic) I42.9
    • in (due to)
  • Myopathy G72.9
    • proximal myotonic (PROMM) G71.11
    • mytonic, proximal (PROMM) G71.11
  • Steinert's disease G71.11
Alongside this code 4 same parent — G71.1
Medications 1

MED-RT files conditions by MeSH, which carves the world differently from ICD-10. These are name matches on this code's description, offered as candidates — not as an assertion that they are this code.

Additional references
AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

Risk adjustment

CMS22HCC76 CMS28HCC197 ESRD21HCC76 ESRD24HCC76

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This code

Billable
yes
Code set
FY2026
Parent
G71.1
Block
G70-G73
Siblings
4

Present FY2024–FY2027.