8C76 Myofibrillar myopathy

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

Myofibrillar myopathies are a heterogeneous group of disorders, characterised by the pathologic finding of myofibrillar disruption on electron microscope with a spectrum of histological abnormalities including excessive desmin accumulation in muscle fibres.

exclusions

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

synonyms

• Myofibrillar myopathy
• MFM - [myofibrillar myopathy]
• Desmin myopathy
• Desmin aggregate myopathy
• Desmin protein surplus myopathy
• Myotilin myopathy
• Myotilinopathy
• Alpha B crystalline myopathy
• Fatal infantile hypertonic myofibrillar myopathy
• Filamin C myopathy
• Filaminopathy
• Z-band alternatively spliced PDZ motif containing-protein myopathy
• ZASP - [Z-band alternatively spliced PDZ motif containing-protein myopathy]
• Zaspopathy
• Certain specified myofibrillar myopathy
• Selcen muscular dystrophy

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