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ICD-10 G71.2 - Congenital myopathies
Chapter 6 Section G70-G73

G71.2

ICD-10 Billable

Congenital myopathies

Inclusion terms:
  • Central core disease
  • Fiber-type disproportion
  • Minicore disease
  • Multicore disease
  • Myotubular (centronuclear) myopathy
  • Nemaline myopathy
Specifically for this code:
  • arthrogryposis multiplex congenita (Q74.3)
From Chapter 6:
  • certain conditions originating in the perinatal period (P04-P96)
  • certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

359.0

ICD-9 Billable

Congenital hereditary muscular dystrophy