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DOID:0070128 - congenital nongoitrous hypothryoidism 6
Disease Ontology Definition:A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1.
Synonyms: CHNG6,
Xenbase Genes : thra
MONDO:0013757 - congenital nongoitrous hypothryoidism 6 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital hypothyroidism (is_a)