Term Name: | thyroid dyshormonogenesis 6 |
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Synonyms: | genetic defect in thyroid hormonogenesis 6, TDH6 |
Definition: | A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1. |
Ontology: | Human Disease [DOID:0112189] ( DOID:0112189 ) |