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DOID:0112189 - thyroid dyshormonogenesis 6
Disease Ontology Definition:A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1.
Synonyms: TDH6, genetic defect in thyroid hormonogenesis 6,
Xenbase Genes : duox2
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee