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AttributesValues
type
sameAs
notation
  • C19.642.482
alternative label
  • Hypoparathyroïdisme
  • Insuffisance parathyroïdienne
  • Hypoparathyroidism
  • Hypoparathyroidism, Idiopathic
  • Hypoparathyroïdie idiopathique
  • Hypoparathyroïdisme idiopathique
  • Idiopathic Hypoparathyroidism
preferred label
  • Hypoparathyroïdie
is in scheme
note
  • A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone
  • A condition of low or absent PTH level and HYPOCALCEMIA. It usually occurs as part of an autoimmune syndrome
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