Central core disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CENTRAL CORE MYOPATHY
MONDO:0007294
RYR1 Causal — ClinVar, GenCC
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Central core disease.
5 View disease cluster →
Benign samaritan congenital myopathy 1 shared geneRYR1 Related via 1 shared gene including RYR1. Congenital multicore myopathy with external ophthalmoplegia 1 shared geneRYR1 Related via 1 shared gene including RYR1. RYR1-related myopathy 1 shared geneRYR1 Related via 1 shared gene including RYR1. Malignant hyperthermia 1 shared geneRYR1 Related via 1 shared gene including RYR1. Sacral agenesis 1 shared geneRYR1 Related via 1 shared gene including RYR1.