Congenital myopathy 4a, 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 4A, autosomal dominant
MONDO_0009711
TPM3 Causal
7704029 24239060 24692096 18300303 17376686 10587521 19953533 19487656 19553118 20951040
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital myopathy 4a, autosomal dominant.
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Congenital generalized hypercontractile muscle stiffness syndrome 1 shared geneTPM3 Related via 1 shared gene including TPM3. Nemaline myopathy 1, autosomal dominant or recessive 1 shared geneTPM3 Related via 1 shared gene including TPM3. Congenital myopathy 4b, autosomal recessive 1 shared geneTPM3 Related via 1 shared gene including TPM3. Cap myopathy 1 shared geneTPM3 Related via 1 shared gene including TPM3. Bladder inflammatory myofibroblastic tumor 1 shared geneTPM3 Related via 1 shared gene including TPM3.