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Summary Literature (1)
MIM:609622 - SHORT QT SYNDROME 3; SQT3

Xenbase Genes: kcnj2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000453 - chromosomal_transposition
MONDO:0012314 - embryonic facial prominence

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