LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Disease: Left ventricular noncompaction ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		0.410 GeneticVariation disease BEFREE Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations. 15219508 2004
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		0.410 GeneticVariation disease CLINVAR
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		0.410 CausalMutation disease CLINVAR
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		0.410 SusceptibilityMutation disease ORPHANET