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Summary Literature (2)
MIM:218700 - HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2; CHNG2

Xenbase Genes: pax8

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019854 - thyroid ectopia
MONDO:0019855 - athyreosis
MONDO:0019860 - thyroid hemiagenesis
MONDO:0019861 - thyroid hypoplasia
MONDO:0024264 - hypothyroidism, congenital, nongoitrous, 2

Disease Ontology (DO):
DOID:0070124 - congenital nongoitrous hypothryoidism 2