G71.3

Mitochondrial myopathy, not elsewhere classified

Billable / specific

G71.3 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Excludes1

Not coded here — never report together with this code.

  • Kearns-Sayre syndrome (H49.81)
  • Leber's disease (H47.21)
  • Leigh's encephalopathy (G31.82)
  • mitochondrial metabolism disorders (E88.4.-)
  • Reye's syndrome (G93.7)

Excludes2

Not included here — may be reported together when both conditions exist.

  • certain conditions originating in the perinatal period (P04-P96) (from G71)
  • certain infectious and parasitic diseases (A00-B99) (from G71)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A) (from G71)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from G71)
  • endocrine, nutritional and metabolic diseases (E00-E88) (from G71)
  • injury, poisoning and certain other consequences of external causes (S00-T88) (from G71)
  • neoplasms (C00-D49) (from G71)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from G71)
  • arthrogryposis multiplex congenita (Q74.3) (from G71)
  • metabolic disorders (E70-E88) (from G71)
  • myositis (M60.-) (from G71)

Also known as

  • Myopathy, mitochondrial NEC

Parent code

  • G71Primary disorders of musclesHeader

Related codes

  • G71.0Muscular dystrophyHeader
  • G71.1Myotonic disordersHeader
  • G71.2Congenital myopathiesHeader
  • G71.8Other primary disorders of musclesBillable
  • G71.9Primary disorder of muscle, unspecifiedBillable

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