dystransthyretinemic hyperthyroxinemia Disease Ontology Browser

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dystransthyretinemic hyperthyroxinemia (DOID:0080219)
Alliance: disease page
Alt IDs: OMIM:145680
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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