Central core disease (Q41401): Difference between revisions
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Revision as of 07:33, 13 August 2026
Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental delay) and is characterised by predominantly proximal weakness, pronounced in the hip girdle.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C72.02 |
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| English | Central core disease |
Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental delay) and is characterised by predominantly proximal weakness, pronounced in the hip girdle. |
