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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