G71.22

Centronuclear myopathy

Non-billable header

G71.22 is a non-billable header code. Use one of the more specific codes below.

Excludes2

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

  • arthrogryposis multiplex congenita (Q74.3) (from G71.2)
  • 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)

Parent code

  • G71.2Congenital myopathiesHeader

More specific codes G71.22

  • G71.220X-linked myotubular myopathyBillable
  • G71.228Other centronuclear myopathyBillable

Related codes

  • G71.20Congenital myopathy, unspecifiedBillable
  • G71.21Nemaline myopathyBillable
  • G71.29Other congenital myopathyBillable

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