congenital myopathy 7A, myosin storage, autosomal dominant
Also known as MSMA, MYH7-related late-onset SPMD, MYH7-related late-onset scapuloperoneal muscular dystrophy, MYH7-related late-onset scapuloperoneal syndrome+10 more
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, myopathy with lysis of type 1 myofibrils, myopathy, hyaline body, autosomal dominant, myopathy, myosin storage, autosomal dominant, scapuloperoneal muscular dystrophy, scapuloperoneal myopathy, MYH7-related, scapuloperoneal syndrome, myopathic type.
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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
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, myopathy with lysis of type 1 myofibrils, myopathy, hyaline body, autosomal dominant, myopathy, myosin storage, autosomal dominant, scapuloperoneal muscular dystrophy, scapuloperoneal myopathy, MYH7-related, scapuloperoneal syndrome, myopathic type
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.