Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7170
Gene Symbol: TPM3
TPM3
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
0.340 Biomarker GENOMICS_ENGLAND Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy. 10619715

1999