Pages that link to "Inborn error of metabolism"
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The following pages link to Inborn error of metabolism:
Displayed 50 items.
- 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)