Pages that link to "Hyperammonemia"
Jump to navigation
Jump to search
The following pages link to Hyperammonemia:
Displayed 134 items.
- Tyrosinemia (← links)
- Ammonia (← links)
- Dystonia (← links)
- Trimethylaminuria (← links)
- Topiramate (← links)
- Angelman syndrome (← links)
- List of diseases (H) (← links)
- Cholesteryl ester storage disease (← links)
- Zellweger syndrome (← links)
- Arginemia (← links)
- Ataxia telangiectasia (← links)
- Batten disease (← links)
- Reye's syndrome (← links)
- Carbamoyl phosphate synthetase I deficiency (← links)
- Carnitine-acylcarnitine translocase deficiency (← links)
- Citrullinemia (← links)
- Glucose-galactose malabsorption (← links)
- Glutathione synthetase deficiency (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hyperlysinemia (← links)
- Hypermethioninemia (← links)
- Hyperprolinemia (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Lysinuric protein intolerance (← links)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (← links)
- N-Acetylglutamate synthase deficiency (← links)
- Ornithine transcarbamylase deficiency (← links)
- Ornithine translocase deficiency (← links)
- Prolidase deficiency (← links)
- Pyruvate carboxylase deficiency (← links)
- Rett syndrome (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Urea cycle disorder (← links)
- Variegate porphyria (← links)
- Methylmalonyl CoA epimerase (← links)
- Methylmalonyl-CoA mutase (← links)
- Glutamate dehydrogenase 1 (← links)
- Ornithine translocase (← links)
- N-Acetylglutamate synthase (← links)
- Ornithine transcarbamylase (← links)
- Mixed disorder of acid-base balance (← links)
- Inborn error of metabolism (← links)
- Causes of hypoglycemia (← links)
- Hyperinsulinemic hypoglycemia (← links)
- Disorders of calcium metabolism (← links)
- Urea cycle (← links)
- Reductive acetyl CoA Pathway (← links)
- Entner-Doudoroff Pathway (← links)
- Wikipedia:Wikiproject Metabolic Pathways/templates (← links)
- Glucose-6-phosphate (← links)
- List of fatty acid metabolism disorders (← links)
- Felbamate (← links)
- Rabeprazole (← links)
- Carglumic acid (← links)
- Gangliosidosis (← links)
- Methylmalonic acidemia (← links)
- Pyruvate dehydrogenase deficiency (← links)
- Renal glycosuria (← links)
- Sialidosis (← links)
- Refsum's disease (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Pseudo-Hurler polydystrophy (← links)
- Hepatoerythropoietic porphyria (← links)
- Aspartylglucosaminuria (← links)
- Cystathioninuria (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- The Living Textbook of Endocrinology (← links)
- The Living Textbook of Metabolic disorders (← links)
- The WikiDoc Living Textbook of Endocrinology (← links)
- The WikiDoc Living Textbook of Metabolic Disorders (← links)
- MT-ATP6 (← links)
- Hyperammonaemia (redirect page) (← links)
- Hepatic failure (← links)
- ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases (← links)
- Valproate (← links)
- Inborn errors of renal tubular transport (← links)
- Hypervalinemia (← links)
- Organic acidemia (← links)
- Carnosinemia (← links)
- Hawkinsinuria (← links)
- Inborn errors of amino acid metabolism (← links)
- D-Glyceric acidemia (← links)
- Urocanic aciduria (← links)
- Amino acid transport disorder (← links)
- Argininemia (← links)
- 2-Hydroxyglutaric aciduria (← links)
- Type I tyrosinemia (← links)
- Type II tyrosinemia (← links)
- Type III tyrosinemia (← links)
- Static popular pages list (← links)
- Encephalopathy causes (← links)
- Early myoclonic encephalopathy (← links)
- High blood ammonia (redirect page) (← links)
- Lesch-Nyhan syndrome differential diagnosis (← links)
- Ataxia telangiectasia differential diagnosis (← links)
- Autism differential diagnosis (← links)
- Ataxia causes (← links)
- Adrenoleukodystrophy differential diagnosis (← links)
- Congenital hyperinsulinism classification (← links)
- Hepatic encephalopathy overview (← links)
- Hepatic encephalopathy history and symptoms (← links)
- WBR0631 (← links)
- Niemann-Pick disease differential diagnosis (← links)
- WBR0970 (← links)
- WBR0976 (← links)
- Topiramate use in specific populations (← links)
- Topiramate drug interactions (← links)
- Topiramate adverse reactions (← links)
- Topiramate warnings and precautions (← links)
- Altered mental status causes (← links)
- Divalproex (← links)
- Glycerol phenylbutyrate (← links)
- Haloperidol (injection) (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- Multiple carboxylase deficiency (← links)
- Propionic acidemia overview (← links)
- Propionic acidemia pathophysiology (← links)
- Propionic acidemia epidemiology and demographics (← links)
- Hepatic encephalopathy other imaging findings (← links)
- Hepatic encephalopathy historical perspective (← links)
- Sandbox:Mental retardation causes (← links)
- Cerebral palsy differential diagnosis (← links)
- Aldehyde dehydrogenase 18 family, member A1 (← links)
- ATP5D (← links)
- TANGO2 (← links)
- ARG1 (gene) (← links)
- Sandbox:Homa (← links)
- MT-ATP8 (← links)
- Fatigue resident survival guide (pediatrics) (← links)
- Template:Metabolic pathway (← links)
- Template:Metabolic pathology (← links)
- Template:Amino acid metabolic pathology (← links)