G71.29

Billable

Other congenital myopathy

G71.29 is the ICD-10-CM code for Other congenital myopathy. It is a billable, specific code valid for reimbursement.

Status
Billable
Chapter
G00-G99
Parent
G71.2
Edition
FY2026

G00-G99 Diseases of the nervous system

What this means — in plain language

MedlinePlus · NIH

What are genetic disorders? Genetic disorders are health conditions caused by changes (also called mutations or variants) in your genes. Genes are parts of DNA found in your cells that carry instructions for how your body grows, develops, and functions. Many genes tell your body how to make proteins, which are needed for your body to work properly. What causes genetic disorders? A genetic disorder happens when a…

Read more about Genetic Disorders at MedlinePlus ↗

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

Includes

  • Central core disease
  • Minicore disease
  • Multicore disease
  • Multiminicore disease

Frequently asked questions

What is ICD-10 code G71.29?
G71.29 is the ICD-10-CM code for "Other congenital myopathy". It falls under G00-G99 Diseases of the nervous system.
Is G71.29 a billable code?
Yes — G71.29 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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