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Summary Literature (0)
DOID:0112186 - thyroid dyshormonogenesis 2A


Disease Ontology Definition:A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TPO on chromosome 2p25.3.

Synonyms: TDH2A, genetic defect in thyroid hormonogenesis 2A, iodide peroxidase deficiency, thyroid peroxidase deficiency

Xenbase Genes : tpo


OMIM:
OMIM:274500 - THYROID DYSHORMONOGENESIS 2A; TDH2A

Other Model Organisms: AGR, 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)