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Summary Literature (0)
OMIM:225250 - HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5


Xenbase Genes: nkx2-5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009154 - hypothyroidism, congenital, nongoitrous, 5
MONDO:0019854 - thyroid ectopia
MONDO:0019855 - athyreosis
MONDO:0019861 - thyroid hypoplasia

Disease Ontology (DO):
DOID:0070125 - congenital nongoitrous hypothryoidism 5