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Summary Literature (0)
MIM:609621 - SHORT QT SYNDROME 2; SQT2

Xenbase Genes: kcnq1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000453 - chromosomal_transposition
MONDO:0012313 - 1st arch maxillary ectoderm

Disease Ontology (DO):
DOID:0050793 - short QT syndrome