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Summary Literature (0)
MIM:115080 - CARDIAC CONDUCTION DEFECT

Xenbase Genes: akap10

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007264 - obsolete sudden cardiac death
MONDO:0019490 - progressive familial heart block

Disease Ontology (DO):
DOID:0111073 - progressive familial heart block