Congenital nemaline myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SEVERE CONGENITAL NEMALINE MYOPATHY
171430C5680451MONDO:0015735
ACTA1 Unknown — Disgenet, GenCC, Orphanet
KLHL40 Unknown
23746549
CTD, Disgenet, Orphanet —
KLHL41 Unknown
24268659
CTD, Disgenet, Orphanet
LMOD3 Unknown
25250574
Disgenet, Orphanet
NEB Unknown — Disgenet, GenCC, Orphanet
All5 Causal0 Unknown5
Related Diseases Diseases that share the most curated genes with Congenital nemaline myopathy.
5 View disease cluster →
Nemaline myopathy 5 shared genesACTA1, LMOD3, NEB, KLHL41, KLHL40 Related via 5 shared genes including ACTA1, LMOD3, NEB. 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 10 1 shared geneLMOD3 Related via 1 shared gene including LMOD3. Nebulin-related myopathy 1 shared geneNEB Related via 1 shared gene including NEB.