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thyroid dyshormonogenesis 6 (DOID:0112189)
Alliance: disease page
Synonyms: 'genetic defect in thyroid hormonogenesis 6'; 'TDH6'
Alt IDs: OMIM:607200
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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last database update
06/14/2022
MGI 6.19
The Jackson Laboratory