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DOID:0070126 - congenital nongoitrous hypothryoidism 1
Disease Ontology Definition:A congenital hypothyroidism that has_material_basis_in mutation in the TSHR gene on chromosome 14q31.
Synonyms: CHNG1, TSH resistance,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0010142 - hypothyroidism due to TSH receptor mutations |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital hypothyroidism (is_a)