MYH7-related skeletal myopathy
Also known as Gowers disease, Laing distal myopathy, Laing early-onset distal myopathy, MPD1+7 more
Gowers disease, Laing distal myopathy, Laing early-onset distal myopathy, MPD1, distal myopathy type 1, myopathy distal, type 1, myopathy, distal, 1, myopathy, distal, early-onset, autosomal dominant, myopathy, distal, type 1, myopathy, late distal hereditary, myosin storage myopathy.
What's happening now
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.
Gowers disease, Laing distal myopathy, Laing early-onset distal myopathy, MPD1, distal myopathy type 1, myopathy distal, type 1, myopathy, distal, 1, myopathy, distal, early-onset, autosomal dominant, myopathy, distal, type 1, myopathy, late distal hereditary, myosin storage myopathy
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.