congenital nongoitrous hypothryoidism 6

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Summary

Literature (0)

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: thra

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013757 - congenital nongoitrous hypothryoidism 6

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)