Pendred syndrome (Q1707822)

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genetic disorder
  • Pendred Syndrome
  • TDH2B
  • congenital hypothyroidism due to dyshormonogenesis 2B
  • deafness with goiter
  • genetic defect in thyroid hormonogenesis 2B
  • goiter-deafness syndrome
  • thyroid dyshormonogenesis 2B
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Language Label Description Also known as
English
Pendred syndrome
genetic disorder
  • Pendred Syndrome
  • TDH2B
  • congenital hypothyroidism due to dyshormonogenesis 2B
  • deafness with goiter
  • genetic defect in thyroid hormonogenesis 2B
  • goiter-deafness syndrome
  • thyroid dyshormonogenesis 2B

Statements

Identifiers

 
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