Nemaline myopathy 1, autosomal dominant or recessive

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Subtype of: Myopathy, autosomal recessive · Nemaline myopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Nemaline myopathy 1, autosomal dominant or recessive
MONDO_0012239
TPM3 Unknown
18300303 24692096
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Nemaline myopathy 1, autosomal dominant or recessive.
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Congenital generalized hypercontractile muscle stiffness syndrome 1 shared geneTPM3 Related via 1 shared gene including TPM3. Congenital myopathy 4a, autosomal dominant 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.