G71.228

Other centronuclear myopathy

Risk-adjusting (HCC)Billable code

HCC risk adjustment mapping

CMS-HCC V28

HCC197

Muscular Dystrophy

CMS-HCC ESRD V24

HCC76

Muscular Dystrophy

Coding notes

Excludes 1 never coded together · Excludes 2 may co-exist

This code · G71.228

Synonyms

Autosomal centronuclear myopathy Autosomal dominant centronuclear myopathy Autosomal recessive centronuclear myopathy Centronuclear myopathy, NOS

Inherited from G71.2Congenital myopathies

Excludes 2

arthrogryposis multiplex congenita (Q74.3)

Inherited from G71Primary disorders of muscles

Excludes 2

arthrogryposis multiplex congenita (Q74.3) metabolic disorders (E70-E88) myositis (M60.-)

Inherited from chapter 6Diseases of the nervous system

Excludes 2

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)

Official Guidelines for G71.228

FY 2026 ›

I.C.6Chapter-specific guidanceChapter 6: Diseases of the Nervous System (G00-G99)

Subsections

Find G71.228 in the alphabetic index

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