(Q50349693)

English

congenital nongoitrous hypothryoidism 3

A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.

  • CHNG3
  • Resistance to Thyrotropin
  • HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
  • HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3; CHNG3
  • Thyrotropin Resistance
  • congenital nongoitrous hypothyroidism 3

Statements

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit