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- B690706d4c91de9f21ca9a58c1ca5aa21 hasDbXref "Orphanet:300751" @default.
- B690706d4c91de9f21ca9a58c1ca5aa21 type Axiom @default.
- B690706d4c91de9f21ca9a58c1ca5aa21 annotatedProperty IAO_0000115 @default.
- B690706d4c91de9f21ca9a58c1ca5aa21 annotatedSource MONDO_0007269 @default.
- B690706d4c91de9f21ca9a58c1ca5aa21 annotatedTarget "Familial dilated cardiomyopathy with conduction defect due to LMNA mutation is a rare familial dilated cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase." @default.