8C72.00 Nemaline myopathy
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Nemaline myopathy encompasses a large spectrum of congenital myopathies characterised by hypotonia, weakness and depressed or absent deep tendon reflexes, with pathologic evidence of nemaline bodies (rods) on muscle biopsy.
synonyms
- Nemaline myopathy
- rod myopathy
- nemaline body disease
- Adult-onset nemaline myopathy
- Amish nemaline myopathy
- Intermediate nemaline myopathy
- Mild nemaline myopathy
- Severe congenital nemaline myopathy
- Typical nemaline myopathy
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