Pages that link to "Lesch–Nyhan syndrome"

The following pages link to Lesch–Nyhan syndrome:

Displaying 31 items.

• L (← links | edit)
• Incontinentia pigmenti (← links | edit)
• Disease (← links | edit)
• Hypotonia (← links | edit)
• List of neurological conditions and disorders (← links | edit)
• Acquired hemophilia A (← links | edit)
• Rett syndrome (← links | edit)
• Inborn errors of metabolism (← links | edit)
• Dictionary of hematology (← links | edit)
• Health topics a-z (← links | edit)
• Health-encyclopedia-L (← links | edit)
• Diseases-and-disorders-L (← links | edit)
• Bloch-sulzberger syndrome (← links | edit)
• Spinal and bulbar muscular atrophy (← links | edit)
• Centronuclear myopathy (← links | edit)
• Adenine phosphoribosyltransferase deficiency (← links | edit)
• Hereditary orotic aciduria without megaloblastic anaemia (← links | edit)
• Orotic aciduria type 1 (← links | edit)
• Medical acronyms (← links | edit)
• Lesch Nyhan syndrome (← links | edit)
• Inborn errors of purine–pyrimidine metabolism (← links | edit)
• Xanthinuria (← links | edit)
• Hereditary xanthinuria (← links | edit)
• Dihydrolipoamide dehydrogenase deficiency (← links | edit)
• Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis (← links | edit)
• Sandboxes (← links | edit)
• Juvenile gout (redirect page) (← links | edit)
  • List of diseases (J) (← links | edit)
• Lesch-Nyhan syndrome (redirect page) (← links | edit)
  • Encyclopedia (← links | edit)
  • Metabolism (← links | edit)
  • Nucleotide salvage (← links | edit)
  • Purine (← links | edit)
  • List of medical terms (← links | edit)
  • Citrullinemia type I (← links | edit)
  • List of rare diseases-L (← links | edit)
  • Aminoacylase 1 deficiency (← links | edit)
  • Abetalipoproteinemia (← links | edit)
  • Hershey bar (← links | edit)
  • D-Glyceric acidemia (← links | edit)
  • Methylmalonyl-CoA mutase deficiency (← links | edit)
  • Succinic semialdehyde dehydrogenase deficiency (← links | edit)
  • Short-chain acyl-coenzyme A dehydrogenase deficiency (← links | edit)
  • Wells-Jankovic syndrome (← links | edit)
  • Glutamate dehydrogenase (← links | edit)
  • Hypoxanthine (← links | edit)
  • Pipecolic acidemia (← links | edit)
  • Chorea-acanthocytosis (← links | edit)
  • AFF2 (← links | edit)
  • Amino acid transport disorder (← links | edit)
  • Hypouricemia (← links | edit)
  • Hyperuricosuria (← links | edit)
  • Purine metabolism (← links | edit)
  • Transphosphoribosidase (← links | edit)
  • Pentosyltransferase (← links | edit)
  • HUPRA syndrome (← links | edit)
  • Histidinuria renal tubular defect syndrome (← links | edit)
  • Nucleic acid metabolism (← links | edit)
  • Fructose bisphosphatase deficiency (← links | edit)
  • Metabolic dysfunction–associated steatotic liver disease (← links | edit)
  • CLCN4 (← links | edit)
  • OPHN1 (← links | edit)
  • UBA1 (← links | edit)
  • SMC1A (← links | edit)
  • 5-Aminoimidazole ribotide (← links | edit)
  • Phosphoribosylamine (← links | edit)
  • William Nyhan (← links | edit)
  • J. Edwin Seegmiller (← links | edit)
  • De novo synthesis (← links | edit)
  • Xanthosine (← links | edit)
  • GSK-789,472 (← links | edit)
  • 2-Hydroxyglutaric aciduria (← links | edit)
• Hypoxanthine guanine phosphoribosyltransferase deficiency (redirect page) (← links | edit)
  • List of diseases (H) (← links | edit)
  • List of rare diseases-H (← links | edit)
  • Genetic diseases-H (← links | edit)
• Template:X-linked disorders (← links | edit)
• Template:Inborn errors of purine–pyrimidine metabolism (← links | edit)