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DOID:0112188 - thyroid dyshormonogenesis 4
Disease Ontology Definition:A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in IYD on chromosome 6q25.1.
Synonyms: TDH4, deiodinase deficiency, genetic defect in thyroid hormonogenesis 4, iodotyrosine dehalogenase deficiency,
Xenbase Genes : iyd
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee