Pages that link to "Homocystinuria"
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The following pages link to Homocystinuria:
Displayed 50 items.
- Chromosome 1 (human) (← links)
- Chromosome 21 (human) (← links)
- Chromosome 5 (human) (← links)
- Dominance relationship (← links)
- Carbamoyl phosphate synthetase I deficiency (← 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)
- N-Acetylglutamate synthase deficiency (← links)
- Ornithine transcarbamylase deficiency (← links)
- Ornithine translocase deficiency (← links)
- Prolidase deficiency (← links)
- Pyruvate carboxylase deficiency (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Urea cycle disorder (← links)
- Variegate porphyria (← links)
- Serine dehydratase (← links)
- Cystathionine beta synthase (← links)
- Mixed disorder of acid-base balance (← links)
- Inborn error of metabolism (← links)
- Disorders of calcium metabolism (← links)
- Reductive acetyl CoA Pathway (← links)
- Entner-Doudoroff Pathway (← links)
- Wikipedia:Wikiproject Metabolic Pathways/templates (← links)
- Glucose-6-phosphate (← links)
- Homocysteine (← links)
- List of fatty acid metabolism disorders (← links)
- Oxidative stress (← links)
- Gangliosidosis (← links)
- Livedoid vasculitis (← links)
- Renal glycosuria (← links)
- Testpage3 (← links)
- Renal vein thrombosis (← links)
- Sialidosis (← links)
- Hyperhomocysteinemia (← links)
- List of amino acid metabolism disorders (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Pseudo-Hurler polydystrophy (← links)
- Genu valgum (← links)
- Pectus carinatum (← links)
- Hepatoerythropoietic porphyria (← links)
- Recessive gene (← links)
- Aspartylglucosaminuria (← links)
- Cystathioninuria (← links)
- Catatonia (← links)