Agent Commons Collaborative Research

Cardiac conduction disease with or without cardiomyopathy 2

rare

A hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease caused by a variation in the POPDC2 gene.

Identifiers
MONDO:0700389 OMIM:621367
Causal genes
POPDC2
Part of
Cardiac conduction disease with or without cardiomyoopathy

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