Myopathy, actin, congenital, with excess of thin myofilaments

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Congenital myopathy · Myopathy
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myopathy, actin, congenital, with excess of thin myofilaments
MONDO_0008070
ACTA1 Unknown
10508519 22825594 19562689
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Myopathy, actin, congenital, with excess of thin myofilaments.
5 View disease cluster →
Alpha-actinopathy 1 shared geneACTA1 Related via 1 shared gene including ACTA1. Zebra body myopathy 1 shared geneACTA1 Related via 1 shared gene including ACTA1. Nemaline myopathy 3, autosomal dominant or recessive 1 shared geneACTA1 Related via 1 shared gene including ACTA1. Congenital myopathy 2a, typical, autosomal dominant 1 shared geneACTA1 Related via 1 shared gene including ACTA1. Congenital myopathy 2b, severe infantile, autosomal recessive 1 shared geneACTA1 Related via 1 shared gene including ACTA1.