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dilated cardiomyopathy 1C

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description A dilated cardiomyopathy that has material basis in mutation in the LDB3 gene on chromosome 10q23.2.
Uniprot Description A form of left ventricular non-compaction, a cardiomyopathy due to myocardial morphogenesis arrest and characterized by a hypertrophic left ventricle, a severely thickened 2-layered myocardium, numerous prominent trabeculations, deep intertrabecular recesses, and poor systolic function. Clinical manifestations are variable. Some affected individuals experience no symptoms at all, others develop heart failure. In some cases, left ventricular non-compaction is associated with other congenital heart anomalies. LVNC3 is an autosomal dominant condition.
Mondo Term and Equivalent IDs
MONDO:0011094:  dilated cardiomyopathy 1C
MESH:C563307: 
NCIT:C170436: