Laron syndrome (Q669822)

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congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration
  • Laron-type isolated somatotropin defect (disorder)
  • Laron-type isolated somatotropin defect
  • Growth Hormone Receptor Deficiency
  • Primary growth hormone resistance
  • Laron-type dwarfism
  • Pituitary Dwarfism 2
  • Growth Hormone Insensitivity Syndrome
  • Primary GH insensitivity
  • Short stature due to growth hormone resistance
  • Complete growth hormone insensitivity
  • Primary GH resistance
  • GH receptor deficiency
  • Primary growth hormone insensitivity
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Language Label Description Also known as
English
Laron syndrome
congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration
  • Laron-type isolated somatotropin defect (disorder)
  • Laron-type isolated somatotropin defect
  • Growth Hormone Receptor Deficiency
  • Primary growth hormone resistance
  • Laron-type dwarfism
  • Pituitary Dwarfism 2
  • Growth Hormone Insensitivity Syndrome
  • Primary GH insensitivity
  • Short stature due to growth hormone resistance
  • Complete growth hormone insensitivity
  • Primary GH resistance
  • GH receptor deficiency
  • Primary growth hormone insensitivity

Statements

Identifiers

MONDO:0009877
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