congenital nongoitrous hypothyroidism 3 Disease Ontology Browser

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Disease Ontology Browser

congenital nongoitrous hypothyroidism 3 (DOID:0070127)
Alliance: disease page
Synonyms: CHNG3
Alt IDs: OMIM:609893, ICD10CM:E03.1
Definition: A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has_material_basis_in variation in the chromosome region 15q25.3-q26.1.

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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