Term Name: dystransthyretinemic hyperthyroxinemia
Synonyms:
Definition: A hyperthyroxinemia that is characterized by an increased affinity for thyroxine (T4) by transthyretin in clinically euthyroid individuals and that has_material_basis_in heterozygous mutation in the TTR gene on chromosome 18q12.
Ontology: Human Disease [DOID:0080219]   ( DOID:0080219 )

Relationships
is a type of: autosomal dominant disease hyperthyroxinemia