Congenital myopathy 7A, myosin storage, autosomal dominant

MONDO:0008409

Also known as: MSMA, MYH7-related late-onset SPMD, MYH7-related late-onset scapuloperoneal muscular dystrophy, MYH7-related late-onset scapuloperoneal syndrome, MYH7-related scapuloperoneal myopathy, SPMD, SPMM, autosomal dominant myosin storage myopathy

14 clinical trials for this condition and its sub-types, 0 tagged with Congenital myopathy 7A, myosin storage, autosomal dominant itself.

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↑ Congenital nervous system disorder (287) ↑ Congenital myopathy (75) ↑ Neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7) (0) ↑ Scapuloperoneal myopathy (0)

Including sub-types (14) Tagged with Congenital myopathy 7A, myosin storage, autosomal dominant (0)

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