Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6261
Gene Symbol: RYR1
RYR1
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
0.400 Biomarker GENOMICS_ENGLAND Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia. 8220423

1993