Misplaced Pages

The following pages link to Ornithine transcarbamylase deficiency

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• Tyrosinemia (links | edit)
• Jesse Gelsinger (links | edit)
• Spinal and bulbar muscular atrophy (links | edit)
• Hartnup disease (links | edit)
• Glutaric aciduria type 1 (links | edit)
• X-linked agammaglobulinemia (links | edit)
• Saccharopinuria (links | edit)
• Ochronosis (links | edit)
• Lysinuric protein intolerance (links | edit)
• Sideroblastic anemia (links | edit)
• Hyperlysinemia (links | edit)
• Dyskeratosis congenita (links | edit)
• X-linked adrenal hypoplasia congenita (links | edit)
• Tetrahydrobiopterin deficiency (links | edit)
• Hermansky–Pudlak syndrome (links | edit)
• Nephrogenic diabetes insipidus (links | edit)
• Argininosuccinic aciduria (links | edit)
• Oculocutaneous albinism (links | edit)
• Glutaric acidemia type 2 (links | edit)
• List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
• Choroideremia (links | edit)
• 2-Hydroxyglutaric aciduria (links | edit)
• 3-Methylglutaconic aciduria (links | edit)
• 6-Pyruvoyltetrahydropterin synthase deficiency (links | edit)
• 3-Methylcrotonyl-CoA carboxylase deficiency (links | edit)
• Methylmalonyl-CoA mutase deficiency (links | edit)
• Glycine encephalopathy (links | edit)
• IPEX syndrome (links | edit)
• Simpson–Golabi–Behmel syndrome (links | edit)
• Hawkinsinuria (links | edit)
• X-linked severe combined immunodeficiency (links | edit)
• Fumarase deficiency (links | edit)
• Aminoaciduria (links | edit)
• Centronuclear myopathy (links | edit)
• Oculocerebrorenal syndrome (links | edit)
• 2-Methylbutyryl-CoA dehydrogenase deficiency (links | edit)
• Histidinemia (links | edit)
• Succinic semialdehyde dehydrogenase deficiency (links | edit)
• ATR-X syndrome (links | edit)
• N-Acetylglutamate synthase deficiency (links | edit)
• Hyperhomocysteinemia (links | edit)
• Hunter syndrome (links | edit)
• Emery–Dreifuss muscular dystrophy (links | edit)
• McLeod syndrome (links | edit)
• Ornithine carbamoyltransferase deficiency disease (redirect page) (links | edit)
  • List of MeSH codes (C18) (links | edit)
  • List of MeSH codes (C16) (links | edit)
  • List of MeSH codes (C10) (links | edit)
  • User:Brainist/MeSH articles (links | edit)
• Ornithine Carbamoyltransferase Deficiency Disease (redirect page) (links | edit)
• Amniotic epithelial cell (links | edit)
• Partial androgen insensitivity syndrome (links | edit)
• Isobutyryl-coenzyme A dehydrogenase deficiency (links | edit)
• X-linked dominant inheritance (links | edit)