Thyroid dyshormonogenesis (Q7799748)

From Wikidata
Jump to navigation Jump to search
Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis
  • dyshormogenetic goiter
  • Thyroid dyshormonogenesis
  • Dyshormonogenesis
  • THYROID DYSHORMONOGENESIS 1; TDH1
  • Iodine Accumulation, Transport, or Trapping Defect
  • THYROID DYSHORMONOGENESIS 1
  • TDH1
  • Hypothyroidism, Congenital, Due to Dyshormonogenesis, 1
  • Thyroid Dyshormonogenesis type 1
  • Thyroid Hormonogenesis, Genetic Defect In, 1
edit
Language Label Description Also known as
English
Thyroid dyshormonogenesis
Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis
  • dyshormogenetic goiter
  • Thyroid dyshormonogenesis
  • Dyshormonogenesis
  • THYROID DYSHORMONOGENESIS 1; TDH1
  • Iodine Accumulation, Transport, or Trapping Defect
  • THYROID DYSHORMONOGENESIS 1
  • TDH1
  • Hypothyroidism, Congenital, Due to Dyshormonogenesis, 1
  • Thyroid Dyshormonogenesis type 1
  • Thyroid Hormonogenesis, Genetic Defect In, 1

Statements

Identifiers

MONDO:0010132
 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit