kodex

Kodex

ICD-10-CM
Code

G71.3

Mitochondrial myopathy, not elsewhere classified

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Hierarchy

  • G00-G99 Diseases of the nervous system (G00-G99)
    • G70-G73 Diseases of myoneural junction and muscle (G70-G73)
      • G71 Primary disorders of muscles
        • G71.0 Muscular dystrophy
        • G71.1 Myotonic disorders
        • G71.2 Congenital myopathies
        • G71.3 Mitochondrial myopathy, not elsewhere classified
        • G71.8 Other primary disorders of muscles
        • G71.9 Primary disorder of muscle, unspecified

Excludes 1

G71.3

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

Excludes 2

G71

  • Q74.3 Arthrogryposis multiplex congenita
  • E70-E88 Metabolic disorders (E70-E88)
  • M60 Myositis

G00-G99

  • certain conditions originating in the perinatal period (P04-P96)
  • A00-B99 Certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
    • O00-O9A Pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
    • Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • S00-T88 Injury, poisoning and certain other consequences of external causes (S00-T88)
  • C00-D49 Neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

Related Terms