Term Name: | congenital nongoitrous hypothyroidism 6 |
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Synonyms: | CHNG6 |
Definition: | A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1. |
Ontology: | Human Disease [DOID:0070128] ( DOID:0070128 ) |