Pages that link to "Homocystinuria"
From WikiMD.com Medical Encyclopedia
The following pages link to Homocystinuria:
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- List of systemic diseases with ocular manifestations (← links | edit)
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- Fanconi syndrome (← links | edit)
- Isovaleric acidemia (← links | edit)
- Waardenburg syndrome (← links | edit)
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- Inborn errors of metabolism (← links | edit)
- Cystinuria (← links | edit)
- Histidinemia (← links | edit)
- Dictionary of rheumatology (← links | edit)
- Fumarase deficiency (← links | edit)
- Health topics a-z (← links | edit)
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- Citrullinemia type I (← links | edit)
- List of rare diseases-H (← links | edit)
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- Encyclopedia-of-medicine-H (← links | edit)
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- Diseases-and-disorders-H (← links | edit)
- MeSH H (← links | edit)
- Template:Amino acid metabolic pathology (← links | edit)
- Saccharopinuria (← links | edit)
- Pectus carinatum (← links | edit)
- Lysinuric protein intolerance (← links | edit)
- Ethylmalonic encephalopathy (← links | edit)
- Carnosinemia (← links | edit)
- Alkaptonuria (← links | edit)
- Aminoacylase 1 deficiency (← links | edit)
- Abetalipoproteinemia (← links | edit)
- Homocystinuria due to MTHFR deficiency (← links | edit)
- Hershey bar (← links | edit)
- Homocystinuria due to CBS deficiency (← links | edit)
- Mild phenylketonuria (← links | edit)
- Carbamoyl phosphate synthetase 1 deficiency (← links | edit)
- Hermansky Pudlak syndrome 2 (← links | edit)
- Prolidase deficiency (← links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (← links | edit)
- D-Glyceric acidemia (← links | edit)
- Glutaric aciduria type 1 (← links | edit)
- Inborn errors of renal tubular transport (← links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links | edit)
- Methylmalonyl-CoA mutase deficiency (← links | edit)