Pages that link to "Inborn error of metabolism"
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The following pages link to Inborn error of metabolism:
Displayed 124 items.
- Tyrosinemia (← links)
- Trimethylaminuria (← links)
- Insulin (← links)
- List of diseases (I) (← links)
- Cholesteryl ester storage disease (← links)
- Newborn screening (← links)
- Arakawa's syndrome II (← links)
- Batten disease (← links)
- Stem cell transplantation (← links)
- Carbamoyl phosphate synthetase I deficiency (← links)
- Congenital disorder of glycosylation (← links)
- Disaccharidase (← links)
- Glucose-galactose malabsorption (← links)
- Glutathione synthetase deficiency (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hereditary fructose intolerance (← links)
- Hyperlysinemia (← links)
- Hypermethioninemia (← links)
- Hyperprolinemia (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Malonyl-CoA decarboxylase deficiency (← 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)
- Sarcosinemia (← links)
- Short-chain acyl-coenzyme A dehydrogenase deficiency (← links)
- Smith-Lemli-Opitz syndrome (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Urea cycle disorder (← links)
- Variegate porphyria (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase (← links)
- Methylmalonyl CoA epimerase (← links)
- Methylcrotonyl-CoA carboxylase (← links)
- L-xylulose reductase (← links)
- Mixed disorder of acid-base balance (← links)
- Glycogen (← links)
- Metabolism (← links)
- Disorders of calcium metabolism (← links)
- Urea cycle (← links)
- Heme (← links)
- List of fatty acid metabolism disorders (← links)
- Ketone (← links)
- Urocanic acid (← links)
- Gangliosidosis (← links)
- Renal glycosuria (← links)
- Congenital disorder (← links)
- Sialidosis (← links)
- Glycogen storage disease (← links)
- Mevalonic aciduria (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Pseudo-Hurler polydystrophy (← links)
- Hepatoerythropoietic porphyria (← links)
- Aspartylglucosaminuria (← links)
- Cystathioninuria (← links)
- Guthrie test (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Urine organic acids (← links)
- Hematopoietic stem cell transplantation (← links)
- Biobanks (← 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)
- Inborn errors of metabolism (redirect page) (← links)
- Hydrops fetalis (← links)
- Genetic disorder (← links)
- Congenital disorder of glycosylation (← links)
- Dihydropyrimidine dehydrogenase deficiency (← links)
- Maple syrup urine disease (← links)
- Ornithine translocase deficiency (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Tetrahydrobiopterin deficiency (← links)
- Urea cycle disorder (← links)
- List of geneticists (← links)
- Medical genetics (← links)
- Metab-L (← links)
- Metabolic disorder (← links)
- Ketotic hypoglycemia (← links)
- Proline (← links)
- List of fatty acid metabolism disorders (← links)
- Abnormal basal metabolic rate (← links)
- Hyperammonemia (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Molecular biology (← links)
- Inborn errors of lipid metabolism (← links)
- Carnosinemia (← links)
- Urocanic aciduria (← links)
- Mental disorder risk factors (← links)
- Mental retardation risk factors (← links)
- Mental retardation screening (← links)
- Autism pathophysiology (← links)
- Pyloric stenosis overview (← links)
- Pyloric stenosis differential diagnosis (← links)
- Inborn error of lipid metabolism (← links)
- WBR0787 (← links)
- Phenylketonuria differential diagnosis (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Sudden infant death syndrome risk factors (← links)
- Sandbox:Asra (← links)
- Vomiting resident survival guide (pediatrics) (← links)
- Jaundice resident survival guide (pediatrics) (← links)
- Cyanosis in newborns (← links)
- Sandbox:Ezici (← links)
- Sandbox:Chelsea (← links)
- Inborn errors (redirect page) (← links)
- Sandbox: TMNG (← links)
- Congenital metabolic disease (redirect page) (← links)
- ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases (← links)
- ETHE1 (← links)
- TMLHE (← links)
- BCKDHA (← links)
- Barraquer-Simons syndrome (← links)
- Inborn errors of renal tubular transport (← links)
- Hypervalinemia (← links)
- Organic acidemia (← links)
- Carnosinemia (← links)
- Metabolic defect (redirect page) (← 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)
- Urologic disease (← links)
- Virus disease (← links)
- Ear disease (← links)
- Fetal disease (← links)
- Inborn errors of purine-pyrimidine metabolism (← links)
- Nervous system disease (← links)
- Type I tyrosinemia (← links)
- Type II tyrosinemia (← links)
- Type III tyrosinemia (← links)
- Inborn errors of carbohydrate metabolism (← links)
- Enzymopathy (redirect page) (← links)
- Hexokinase deficiency (← links)
- Sweat gland disease (← links)
- Menkes disease (patient information) (← links)
- Inborn metabolic disorders (redirect page) (← links)
- Hypoglycemia overview (← links)
- Hypoglycemia causes (← links)
- Hypoglycemia primary prevention (← links)
- Mental retardation physical examination (← links)
- Cyanosis causes (← links)
- Lactic acidosis classification (← links)
- WBR0302 (← links)
- WBR1018 (← links)
- Levocarnitine (oral) (← links)
- Levocarnitine (injection) (← links)
- Smith–Lemli–Opitz syndrome (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- Differentiating Hypoglycemia from other diseases (← links)
- Neurological symptoms in neonates (← links)
- Cyanosis resident survival guide (← links)
- Template:Metabolic pathology (← links)
- Template:Amino acid metabolic pathology (← links)
- Template:Lipidemias (← links)
- Template:Other metabolic pathology (← links)
- Template:Lipid metabolism disorders (← links)
- Template:Inborn errors of carbohydrate metabolism (← links)
- Template:Medical conditions (← links)