Centronuclear myopathy (Q41397): Difference between revisions
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13 August 2026
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Latest revision as of 07:33, 13 August 2026
Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinical features of a congenital myopathy and centrally placed nuclei on muscle biopsy. It encompasses the X-linked form, the autosomal recessive form and the autosomal dominant form with a highly variable clinical presentation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C72.01 |
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| English | Centronuclear myopathy |
Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinical features of a congenital myopathy and centrally placed nuclei on muscle biopsy. It encompasses the X-linked form, the autosomal recessive form and the autosomal dominant form with a highly variable clinical presentation. |
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CID11:8C72.01
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dki-india-8C72.01
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Concluído
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13 August 2026
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