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Summary Literature (4)
MIM:274600 - PENDRED SYNDROME; PDS

Xenbase Genes: slc26a4.3, slc26a4, slc26a4.2, kcnj10, foxi1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010134 - secretory circumventricular organ

Disease Ontology (DO):
DOID:0060744 - Pendred Syndrome