Pages that link to "Oculocutaneous albinism"
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The following pages link to Oculocutaneous albinism:
Displaying 45 items.
- Tyrosinemia (← links)
- Pallor (← links)
- Trimethylaminuria (← links)
- Vision loss (← links)
- Glutathione synthetase deficiency (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hyperlysinemia (← links)
- Hypermethioninemia (← links)
- Hyperprolinemia (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Ornithine translocase deficiency (← links)
- Prolidase deficiency (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Urea cycle disorder (← links)
- Inborn error of metabolism (← links)
- Melanin (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- TYRP1 (← links)
- OCA2 (← links)
- SLC45A2 (← 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)
- Albinism (patient information) (← links)
- Albinism overview (← links)
- Albinism classification (← links)
- Albinism pathophysiology (← links)
- Albinism epidemiology and demographics (← links)
- Albinism physical examination (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- Differentiating Albinism from other diseases (← links)
- Template:Amino acid metabolic pathology (← links)