thyroid dyshormonogenesis 5 Disease Ontology Browser

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thyroid dyshormonogenesis 5 (DOID:0112184)
Alliance: disease page
Synonyms: genetic defect in thyroid hormonogenesis 5; TDH5
Alt IDs: OMIM:274900, MESH:C562771
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOXA2 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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