2017/18 ICD-10-CM Diagnosis Code G71.2

Congenital myopathies

Applicable To
  • Central core disease
  • Fiber-type disproportion
  • Minicore disease
  • Multicore disease
  • Myotubular (centronuclear) myopathy
  • Nemaline myopathy
Type 1 Excludes
Type 1 Excludes Help
A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as G71.2. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
  • arthrogryposis multiplex congenita (
    ICD-10-CM Diagnosis Code Q74.3

    Arthrogryposis multiplex congenita

      2016 2017 2018 Billable/Specific Code POA Exempt
    Q74.3
    )
The following code(s) above G71.2 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to G71.2:
  • G00-G99
    2018 ICD-10-CM Range G00-G99

    Diseases of the nervous system

    Type 2 Excludes
    • 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)
    Diseases of the nervous system
  • G71
    ICD-10-CM Diagnosis Code G71

    Primary disorders of muscles

      2016 2017 2018 Non-Billable/Non-Specific Code
    Type 2 Excludes
    • arthrogryposis multiplex congenita (Q74.3)
    • metabolic disorders (E70-E88)
    • myositis (M60.-)
    Primary disorders of muscles
Approximate Synonyms Clinical Information ICD-10-CM G71.2 is grouped within Diagnostic Related Group(s) (MS-DRG v35.0):

Convert G71.2 to ICD-9-CM

Code History

Diagnosis Index entries containing back-references to G71.2:

ICD-10-CM Codes Adjacent To G71.2
G70.89 Other specified myoneural disorders
G70.9 Myoneural disorder, unspecified
G71 Primary disorders of muscles
G71.0 Muscular dystrophy
G71.1 Myotonic disorders
G71.11 Myotonic muscular dystrophy
G71.12 Myotonia congenita
G71.13 Myotonic chondrodystrophy
G71.14 Drug induced myotonia
G71.19 Other specified 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
G72 Other and unspecified myopathies
G72.0 Drug-induced myopathy
G72.1 Alcoholic myopathy
G72.2 Myopathy due to other toxic agents
G72.3 Periodic paralysis
G72.4 Inflammatory and immune myopathies, not elsewhere classified
G72.41 Inclusion body myositis [IBM]

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.