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Summary Literature (0)
OMIM:614450 - HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6


Xenbase Genes: thra

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013757 - congenital nongoitrous hypothryoidism 6
MONDO:0019995 - peripheral resistance to thyroid hormones

Disease Ontology (DO):
DOID:0070128 - congenital nongoitrous hypothryoidism 6