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Summary Literature (0)
DOID:0070127 - congenital nongoitrous hypothryoidism 3

Disease Ontology 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.

Synonyms: CHNG3,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012360 - congenital nongoitrous hypothryoidism 3


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)