About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/10/2020
MGI 6.16
The Jackson Laboratory