Nemaline myopathy 5c, autosomal dominant

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Subtype of: Nemaline myopathy · Nemaline myopathy 5
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Nemaline myopathy 5C, autosomal dominant
MONDO_0957284
TNNT1 Causal
29178646 35510366
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Nemaline myopathy 5c, autosomal dominant.
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Amish nemaline myopathy 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Nemaline myopathy 5 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Nemaline myopathy 5a, autosomal recessive, severe infantile 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Childhood-onset nemaline myopathy 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Nemaline myopathy 1 shared geneTNNT1 Related via 1 shared gene including TNNT1.