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Echinobase
Summary Literature (0)
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: deiodinase deficiency, genetic defect in thyroid hormonogenesis 4, iodotyrosine dehalogenase deficiency, TDH4

Echinobase Genes : iyd


MIM:
MIM:274800 - thyroid dyshormonogenesis 4; tdh4

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)