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thyroid dyshormonogenesis 1 (DOID:0112185)
Alliance: disease page
Synonyms: genetic defect in thyroid hormonogenesis 1; iodide accumulation, transport, or trapping defect; TDH1
Alt IDs: OMIM:274400, MESH:C564766
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in SLC5A5 on chromosome 19p13.11.

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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11/12/2024
MGI 6.24 		The Jackson Laboratory