Childhood-onset nemaline myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
childhood-onset nemaline myopathy
MONDO_0015023MONDO_0957281
MYPN Unknown
28017374
Open Targets
TNNI1 Unknown — ClinGen
TNNT1 Unknown
35165004 35510366 31970803
Open Targets
All3 Causal0 Unknown3
Related Diseases Diseases that share the most curated genes with Childhood-onset nemaline myopathy.
5 View disease cluster →
Dilated cardiomyopathy 1KK 1 shared geneMYPN Related via 1 shared gene including MYPN. Nemaline myopathy 11, autosomal recessive 1 shared geneMYPN Related via 1 shared gene including MYPN. 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.