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Summary Literature (1)
DOID:0050328 - congenital hypothyroidism

Disease Ontology Definition:A hypothyroidism that is present at birth.

Synonyms: cretinism,

Xenbase Genes : pax8, tshb, slc5a5, nkx2-5, tpo, iyd, tshr, thra, duox2, tg

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018612 - congenital hypothyroidism

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypothyroidism (is_a), physical disorder (is_a)