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Summary Literature (0)
DOID:0112184 - thyroid dyshormonogenesis 5

Disease Ontology Definition:A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOXA2 on chromosome 15q21.1.

Synonyms: genetic defect in thyroid hormonogenesis 5, TDH5

Xenbase Genes : duoxa2


MIM:
MIM:274900 - THYROID DYSHORMONOGENESIS 5; TDH5

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal recessive disease (is_a), familial thyroid dyshormonogenesis (is_a)