Phenylketonuria/Related Articles: Difference between revisions
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imported>Chris Day (New page: {{subpages}} <!-- INSTRUCTIONS, DELETE AFTER READING: Related Articles pages link to existing and proposed articles that are related to the present article. These lists of links double as...) |
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{{r|Maple syrup urine disease||**}} | {{r|Maple syrup urine disease||**}} | ||
{{r|Medium-chain acyl-CoA dehydrogenase deficiency||**}} | {{r|Medium-chain acyl-CoA dehydrogenase deficiency||**}} | ||
{{r|Methylmalonic acidemia | {{r|Methylmalonic acidemia (CBLAB)||**}} | ||
{{r|Methylmalonic acidemia (MUT)||**}} | |||
{{r|Methylmalonic acidemia||**}} | |||
{{r|Multiple carboxylase deficiency||**}} | {{r|Multiple carboxylase deficiency||**}} | ||
{{r|Propionic acidemia||**}} | {{r|Propionic acidemia||**}} | ||
{{r|Sickle cell anemia||**}} | {{r|Sickle cell anemia||**}} | ||
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{{r|Tyrosinemia type I||**}} | {{r|Tyrosinemia type I||**}} | ||
{{r|Very long-chain acyl-CoA dehydrogenase deficiency||**}} | {{r|Very long-chain acyl-CoA dehydrogenase deficiency||**}} | ||
==Articles related by keyphrases (Bot populated)== | |||
{{r|Pachygyria}} | |||
{{r|Federalist Party}} | |||
{{r|Phenylalanine}} | |||
Latest revision as of 12:00, 3 October 2024
- See also changes related to Phenylketonuria, or pages that link to Phenylketonuria or to this page or whose text contains "Phenylketonuria".
Parent topics
Subtopics
- Newborn screening [r]: Add brief definition or description
- 3-Methylcrotonyl-CoA carboxylase deficiency [r]: Add brief definition or description
- Argininosuccinic acidemia [r]: Add brief definition or description
- Beta-Ketothiolase deficiency [r]: Add brief definition or description
- Biotinidase deficiency [r]: Add brief definition or description
- Carnitine uptake defect [r]: Add brief definition or description
- Citrullinemia [r]: Add brief definition or description
- Classical galactosemia [r]: Add brief definition or description
- Congenital adrenal hyperplasia [r]: Add brief definition or description
- Congenital hypothyroidism [r]: Add brief definition or description
- Cystic fibrosis [r]: Add brief definition or description
- Glutaric acidemia type I [r]: Add brief definition or description
- Hb S/Beta-Thalassemia [r]: Add brief definition or description
- Homocystinuria [r]: Hereditary disease characterized by a deficiency of the enzyme serine dehydratase, causing genetic defects. [e]
- HMG-CoA lyase deficiency [r]: Add brief definition or description
- Isovaleric acidemia [r]: Add brief definition or description
- Long-chain 3-OH acyl-CoA dehydrogenase deficiency [r]: Add brief definition or description
- Maple syrup urine disease [r]: Add brief definition or description
- Medium-chain acyl-CoA dehydrogenase deficiency [r]: Add brief definition or description
- Methylmalonic acidemia (CBLAB) [r]: Add brief definition or description
- Methylmalonic acidemia (MUT) [r]: Add brief definition or description
- Multiple carboxylase deficiency [r]: Add brief definition or description
- Propionic acidemia [r]: Add brief definition or description
- Sickle cell anemia [r]: Add brief definition or description
- Trifunctional protein deficiency [r]: Add brief definition or description
- Tyrosinemia type I [r]: Add brief definition or description
- Very long-chain acyl-CoA dehydrogenase deficiency [r]: Add brief definition or description