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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
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee