Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
0.390 Biomarker GENOMICS_ENGLAND Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies. 23413262

2013