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Summary Literature (0)
MIM:616749 - HETEROTAXY, VISCERAL, 7, AUTOSOMAL; HTX7

Xenbase Genes: mmp21

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014762 - heterotaxy, visceral, 7, autosomal
MONDO:0018677 - visceral heterotaxy