Nemaline myopathy 3, autosomal dominant or recessive

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Myopathy, autosomal recessive · Nemaline myopathy
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Nemaline myopathy 3, autosomal dominant or recessive
MONDO_0008070
ACTA1 Causal
24642510 20179953 25913210 26436962 25182138 22825594 19562689 30266093 10508519 21570694 30354303 26888179 30195123 16945537 32969603
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Nemaline myopathy 3, autosomal dominant or recessive.
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. Myopathy, actin, congenital, with excess of thin myofilaments 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.