(Q727436)

English

Lesch–Nyhan syndrome

rare genetic syndrome

  • Complete hypoxanthine-guanine phosphoribosyltransferase deficiency
  • HG-PRT deficiency
  • Hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder)
  • Hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder) [Ambiguous]
  • Hypoxanthine-guanine-phosphoribosyltransferase deficiency (& [Lesch - Nyhan syndrome])
  • Lesch - Nyhan syndrome
  • Lesch-Nyhan syndrome (disorder)
  • X-linked hyperuricemia (disorder) [Ambiguous]
  • deficiency of IMP pyrophosphorylase
  • hypoxanthine guanine phosphoribosyltransferase deficiency
  • Lesch-Nyhan syndrome, LNS
  • Hypoxanthine-guanine phosphoribosyltransferase deficiency
  • X-linked hyperuricemia
  • Hypoxanthine-guanine-phosphoribosyltransferase deficiency

Statements

Identifiers

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5C55.01
Lesch-Nyhan syndrome
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