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G71.220

Billable

X-linked myotubular myopathy

G71.220 is the ICD-10-CM code for X-linked myotubular 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

X-linked myotubular myopathy is a condition that primarily affects muscles used for movement (skeletal muscles) and occurs almost exclusively in males. People with this condition have muscle weakness (myopathy) and decreased muscle tone (hypotonia) that are usually evident at birth. When viewed under a microscope, the muscle fibers of affected individuals are typically small and underdeveloped. The muscle problems…

Read more about X-linked myotubular myopathy at MedlinePlus ↗

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

Includes

  • •Myotubular (centronuclear) myopathy

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 G71.220?
G71.220 is the ICD-10-CM code for "X-linked myotubular myopathy". It falls under G00-G99 Diseases of the nervous system.
Is G71.220 a billable code?
Yes — G71.220 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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