Term Name: thyroid dyshormonogenesis 3
Synonyms: genetic defect in thyroid hormonogenesis 3, TDH3
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.
Ontology: Human Disease [DOID:0112187]   ( DOID:0112187 )

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