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Summary Literature (0)
DOID:0112187 - thyroid dyshormonogenesis 3


Disease Ontology Definition:A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.

Synonyms: TDH3, genetic defect in thyroid hormonogenesis 3

In OMIM:
OMIM:274700 - THYROID DYSHORMONOGENESIS 3; TDH3


Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tg

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), familial thyroid dyshormonogenesis (is_a)