08Diseases of the nervous system
Diseases of neuromuscular junction or muscle
Primary disorders of muscles
8C72Congenital myopathies
8C72.0Congenital myopathy with structural abnormalities
8C72.00
category
Nemaline myopathy
Definition 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.
Also indexed as
Adult-onset nemaline myopathy Amish nemaline myopathy Intermediate nemaline myopathy Mild nemaline myopathy Nemaline myopathy Severe congenital nemaline myopathy Typical nemaline myopathy nemaline body disease rod myopathy
Nearby in Congenital myopathy with structural abnormalities
International Classification of Diseases, Eleventh Revision (ICD-11), World Health Organization (WHO) 2019/2021, https://icd.who.int/browse11. Licensed under Creative Commons Attribution-NoDerivatives 3.0 IGO (CC BY-ND 3.0 IGO).
Release 2026-01.
View this entity in the official WHO ICD-11 browser .
This page reproduces WHO classification content for reference. It is not
medical advice and must not be used to diagnose or treat. For coding
decisions, consult the official release and your national coding guidelines.
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