Visualize Submit Comment
Metadata
ID DOID:0080219
Name dystransthyretinemic hyperthyroxinemia
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.
https://pubmed.ncbi.nlm.nih.gov/1979335/
Xrefs

OMIM:145680

Parent Relationships

is_a hyperthyroxinemia

is_a autosomal dominant disease

Add an item to the term tracker