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Disease Ontology Browser
congenital nongoitrous hypothyroidism 6 (DOID:0070128)
Alliance: disease page
Synonyms: CHNG6
Alt IDs: OMIM:614450, ICD10CM:E03.1
Definition: A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1.

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