Term Name:	thyroid dyshormonogenesis 5
Synonyms:	genetic defect in thyroid hormonogenesis 5, TDH5
Definition:	A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOXA2 on chromosome 15q21.1.
Ontology:	Human Disease [DOID:0112184]   ( DOID:0112184 )