LDB3, LIM domain binding 3, 11155

N. diseases: 69; N. variants: 15
Disease: Myofibrillar Myopathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		0.410 GeneticVariation disease BEFREE In all SAMP strains except SAMP8, we detected a p.R473W missense mutation in the Ldb3 gene, which has been associated with myofibrillar myopathy. 23586671 2013
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		0.410 CausalMutation disease CLINVAR
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		0.410 Biomarker disease HPO
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		0.410 Biomarker disease CTD_human