Nemaline myopathy 10

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Subtype of: Nemaline myopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Nemaline myopathy 10
MONDO_0014513
LMOD3 Causal
25250574 28815944 29331079 30291184 30642739 31572445 32008911 33820833
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Nemaline myopathy 10.
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Congenital nemaline myopathy 1 shared geneLMOD3 Related via 1 shared gene including LMOD3. Nemaline myopathy 1 shared geneLMOD3 Related via 1 shared gene including LMOD3. Joubert syndrome 1 shared geneLMOD3 Related via 1 shared gene including LMOD3. Alzheimer disease 1 shared geneLMOD3 Related via 1 shared gene including LMOD3.