Term Name: thyroid dyshormonogenesis 6
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 )

Relationships
is a type of: autosomal recessive disease familial thyroid dyshormonogenesis