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thyroid dyshormonogenesis 6 (DOID:0112189)
Alliance: disease page
Synonyms: genetic defect in thyroid hormonogenesis 6; TDH6
Alt IDs: OMIM:607200, MESH:C564608
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1.

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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory