Congenital myopathy 2c, severe infantile, autosomal dominant

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Subtype of: Congenital myopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Congenital myopathy 2C, severe infantile, autosomal dominant
MONDO_0859523
ACTA1 Causal
17387733 15468086
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital myopathy 2c, severe infantile, autosomal dominant.
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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. 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.