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Summary Literature (0)
DOID:0070124 - congenital nongoitrous hypothyroidism 2

Disease Ontology Definition:A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the PAX8 gene on chromosome 2q13.

Synonyms: CHNG2, congenital hypothyroidism due to thyroid dysgenesis or hypoplasia

Xenbase Genes : pax8

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0024264 - hypothyroidism, congenital, nongoitrous, 2


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), congenital hypothyroidism (is_a)