Congenital fiber-type disproportion myopathy
Also known as CFTDM, congenital fiber-type disproportion, congenital myopathy with fiber type disproportion, congenital myopathy with fibre type disproportion+3 more
CFTDM, congenital fiber-type disproportion, congenital myopathy with fiber type disproportion, congenital myopathy with fibre type disproportion, congenital fiber type disproportion, congenital fibre type disproportion, myopathy, congenital with fiber-type disproportion.
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.
CFTDM, congenital fiber-type disproportion, congenital myopathy with fiber type disproportion, congenital myopathy with fibre type disproportion, congenital fiber type disproportion, congenital fibre type disproportion, myopathy, congenital with fiber-type disproportion
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.