thyroid dyshormonogenesis 3 Disease Ontology Browser

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Disease Ontology Browser

thyroid dyshormonogenesis 3 (DOID:0112187)
Alliance: disease page
Synonyms: genetic defect in thyroid hormonogenesis 3; TDH3
Alt IDs: OMIM:274700, MESH:C562769
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.

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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