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thyroid dyshormonogenesis 2A (DOID:0112186)
Alliance: disease page
Synonyms: genetic defect in thyroid hormonogenesis 2A; iodide peroxidase deficiency; TDH2A; thyroid peroxidase deficiency
Alt IDs: OMIM:274500, MESH:C563206
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TPO on chromosome 2p25.3.


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
02/13/2024
MGI 6.23
The Jackson Laboratory