Congenital lethal myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL LETHAL MYOPATHY COMPTON NORTH TYPE
C4750773
CNTN1 Unknown — Disgenet
CONGENITAL LETHAL MYOPATHY, COMPTON-NORTH TYPE
210163
CNTN1 Unknown
19026398
Orphanet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital lethal myopathy .
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Compton-north congenital myopathy 1 shared geneCNTN1 Related via 1 shared gene including CNTN1. Spondylosis 1 shared geneCNTN1 Related via 1 shared gene including CNTN1. Congenital myopathy 1 shared geneCNTN1 Related via 1 shared gene including CNTN1. Dry eye syndrome 1 shared geneCNTN1 Related via 1 shared gene including CNTN1. Astrocytoma 1 shared geneCNTN1 Related via 1 shared gene including CNTN1.