congenital nongoitrous hypothryoidism 6 (Q50349694)

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A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1.
  • CHNG6
  • HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6
  • HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6
  • Hypothyroidism, Congenital, Nongoitrous, type 6
  • congenital nongoitrous hypothyroidism 6
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Language Label Description Also known as
English
congenital nongoitrous hypothryoidism 6
A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1.
  • CHNG6
  • HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6
  • HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6
  • Hypothyroidism, Congenital, Nongoitrous, type 6
  • congenital nongoitrous hypothyroidism 6

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