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Summary Literature (0)
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: genetic defect in thyroid hormonogenesis 6, TDH6

Xenbase Genes : duox2


MIM:
MIM:607200 - THYROID DYSHORMONOGENESIS 6; TDH6

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), familial thyroid dyshormonogenesis (is_a)