8C72.0 Congenital myopathy with structural abnormalities

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry.

exclusions

• Secondary myopathies  (8C80-8C8Z)
• Myasthenia gravis or certain specified neuromuscular junction disorders  (8C60-8C6Z)

sections/codes in this section (8C72.0-8C72.0)

• Nemaline myopathy  (8C72.00)
• Centronuclear myopathy  (8C72.01)
• Central core disease  (8C72.02)
• Other specified congenital myopathy with structural abnormalities  (8C72.0Y)
• Congenital myopathy with structural abnormalities, unspecified  (8C72.0Z)

postcoordination

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