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Disease Ontology Browser
congenital nongoitrous hypothyroidism 1 (DOID:0070126)
Alliance: disease page
Synonyms: CHNG1; TSH resistance
Alt IDs: OMIM:275200, ICD10CM:E03.1
Definition: A congenital hypothyroidism that has_material_basis_in mutation in the TSHR gene on chromosome 14q31.

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
MGI 6.19
The Jackson Laboratory