Variants
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Multiminicore myopathy

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Description

A rare hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy.

ORDO

  • Mode of Inheritance

    VARIANTS

    60

    SEE THE VARIANTS →

    Genes

    External Links

    • OMIM
    • Orphanet

      598

    • HPO
    • Medgen

      C0270962

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