| Term Name: | congenital nongoitrous hypothyroidism 6 |
|---|---|
| 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 ) |