Misplaced Pages

The following pages link to Ornithine transcarbamylase deficiency

• (link count
• transclusion count
• sorted list) · See help page for transcluding these entries

Showing 50 items.

• Gene therapy (links | edit)
• Phenylketonuria (links | edit)
• Diabetes insipidus (links | edit)
• Androgen insensitivity syndrome (links | edit)
• Adrenoleukodystrophy (links | edit)
• Fragile X syndrome (links | edit)
• Pelizaeus–Merzbacher disease (links | edit)
• Rett syndrome (links | edit)
• Ornithine (links | edit)
• Alkaptonuria (links | edit)
• Haemophilia A (links | edit)
• Haemophilia B (links | edit)
• Barth syndrome (links | edit)
• Ornithine transcarbamylase (links | edit)
• Glucose-6-phosphate dehydrogenase deficiency (links | edit)
• Occipital horn syndrome (links | edit)
• Methylmalonic acidemias (links | edit)
• Propionic acidemia (links | edit)
• Hyperammonemia (links | edit)
• Waardenburg syndrome (links | edit)
• Chronic granulomatous disease (links | edit)
• Homocystinuria (links | edit)
• Blood urea nitrogen (links | edit)
• Alport syndrome (links | edit)
• Newborn screening (links | edit)
• MASA syndrome (links | edit)
• Aicardi syndrome (links | edit)
• Duchenne muscular dystrophy (links | edit)
• Cystinuria (links | edit)
• Becker muscular dystrophy (links | edit)
• Kallmann syndrome (links | edit)
• Lesch–Nyhan syndrome (links | edit)
• Menkes disease (links | edit)
• Inborn errors of metabolism (links | edit)
• Ornithine Transcarbamylase Deficiency (redirect page) (links | edit)
  • Cat coat genetics (links | edit)
  • User:MtB (links | edit)
  • User:The Anome/Compassionate allowance conditions (links | edit)
• Wiskott–Aldrich syndrome (links | edit)
• Incontinentia pigmenti (links | edit)
• X-linked recessive inheritance (links | edit)
• Sex linkage (links | edit)
• Coffin–Lowry syndrome (links | edit)
• Trimethylaminuria (links | edit)
• Isovaleric acidemia (links | edit)
• Maple syrup urine disease (links | edit)
• Orotic acid (links | edit)
• X-linked ichthyosis (links | edit)
• Cystinosis (links | edit)
• Citrullinemia (links | edit)
• Beta-ketothiolase deficiency (links | edit)
• Norrie disease (links | edit)
• 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)