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G71.228

Billable

Other centronuclear myopathy

G71.228 is the ICD-10-CM code for Other centronuclear myopathy. It is a billable, specific code valid for reimbursement.

Status
Billable
Chapter
G00-G99
Parent
G71.22
Edition
FY2026

G00-G99 Diseases of the nervous system

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What this means — in plain language

MedlinePlus · NIH

Centronuclear myopathy is a condition characterized by muscle weakness (myopathy) and wasting (atrophy) in the skeletal muscles, which are the muscles used for movement. The severity of centronuclear myopathy varies among affected individuals, even among members of the same family. People with centronuclear myopathy begin experiencing muscle weakness at any time from birth to early adulthood. The muscle weakness…

Read more about Centronuclear myopathy at MedlinePlus ↗

Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.

Includes

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

Medications indicated for this condition

FDA labeling

Drugs whose FDA labeling lists this condition's category among its indications. Informational only — not a treatment recommendation or medical advice.

Conditions mapped to this code

MedlinePlus · NIH
Muscular DystrophyMitochondrial Diseases

Plain-language health-topic references grounded in MedlinePlus (NIH/NLM).

Benefits & assistance programs

Federal & state

Assistance programs whose eligibility maps to this condition's category. Informational only — eligibility is determined by the administering agency.

Frequently asked questions

What is ICD-10 code G71.228?
G71.228 is the ICD-10-CM code for "Other centronuclear myopathy". It falls under G00-G99 Diseases of the nervous system.
Is G71.228 a billable code?
Yes — G71.228 is a billable, specific ICD-10-CM code valid for reimbursement.

Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.

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