Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4703
Gene Symbol: NEB
NEB
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		0.360 Biomarker GENOMICS_ENGLAND Mutations in the nebulin gene can cause severe congenital nemaline myopathy. 12207937

2002