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G71.2 - Congenital myopathies


The ICD 10 Code for Congenital myopathies is listed as G71.2.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field Value
Diagnosis Code: G71.2
Description: Congenital myopathies
  • Central core disease
  • Fiber-type disproportion
  • Minicore disease
  • Multicore disease
  • Myotubular (centronuclear) myopathy
  • Nemaline myopathy
  • Excludes1: arthrogryposis multiplex congenita (Q74.3)
Diagnostic Related Groups
(MS-DRG v30.0)
091 - Other Disorders Of Nervous System W Mcc
092 - Other Disorders Of Nervous System W Cc
093 - Other Disorders Of Nervous System W/o Cc/mcc
Chapter Diseases of the nervous system (G00-G99)
Block Diseases of myoneural junction and muscle (G70-G73)
Parent G71 - Primary disorders of muscles
ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD 9 Dx Code: 359.0 - Congenital hereditary muscular dystrophy (approximate)
ICD-10-CM Siblings (same level / similar specificity) of G71.2:
G71.0 - Muscular dystrophy
G71.1 - Myotonic disorders
G71.3 - Mitochondrial myopathy, not elsewhere classified
G71.8 - Other primary disorders of muscles
G71.9 - Primary disorder of muscle, unspecified