The following pages link to Systemic primary carnitine deficiency
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Adrenoleukodystrophy (links | edit)
- List of diseases (C) (links | edit)
- Carnitine (links | edit)
- Propionic acidemia (links | edit)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- Inborn errors of metabolism (links | edit)
- Fatty acid metabolism (links | edit)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (links | edit)
- Beta oxidation (links | edit)
- Carnitine uptake defect (redirect page) (links | edit)
- Carnitine uptake deficiency (redirect page) (links | edit)
- Renal carnitine transport defect (redirect page) (links | edit)
- Systemic carnitine deficiency (redirect page) (links | edit)
- Inborn error of lipid metabolism (links | edit)
- Carnitine palmitoyltransferase I deficiency (links | edit)
- Carnitine palmitoyltransferase II deficiency (links | edit)
- Carnitine-acylcarnitine translocase deficiency (links | edit)
- Mitochondrial trifunctional protein deficiency (links | edit)
- Very long-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- Muscle carnitine palmityltransferase deficiency (redirect page) (links | edit)
- Biotinidase deficiency (links | edit)
- Glutaric acidemia type 2 (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Malonic aciduria (links | edit)
- Short-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- 2,4 Dienoyl-CoA reductase deficiency (links | edit)
- Carnitine deficiency (redirect page) (links | edit)
- Sjögren–Larsson syndrome (links | edit)
- Acute fatty liver of pregnancy (links | edit)
- 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (links | edit)
- SLC22A5 (links | edit)
- Major facilitator superfamily (links | edit)
- Metabolic myopathy (links | edit)
- Fatty-acid metabolism disorder (links | edit)
- Hereditary carnitine deficiency (redirect page) (links | edit)
- Carnitin Transporter Deficiency (redirect page) (links | edit)
- Primary carnitine deficiency (redirect page) (links | edit)
- Inborn error of lipid metabolism (links | edit)
- Carnitine palmitoyltransferase I deficiency (links | edit)
- Carnitine palmitoyltransferase II deficiency (links | edit)
- Carnitine-acylcarnitine translocase deficiency (links | edit)
- Chromosome 5 (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Organic cation transport protein (links | edit)
- SLC22A5 (links | edit)
- Cud (disambiguation) (links | edit)
- Talk:Reye syndrome (links | edit)
- User:SnuBru44/sandbox (links | edit)
- Carnitine transporter deficiency (redirect page) (links | edit)
- Deficiency of plasma-membrane carnitine transporter (redirect page) (links | edit)
- Hereditary carnitine deficiency syndrome (redirect to section "Genetics") (links | edit)
- Talk:Systemic primary carnitine deficiency (transclusion) (links | edit)
- User:Juntilla87/sandbox (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages (links | edit)
- User:Drsalmanshah165/Books/Anaphylaxis (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-c (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-C (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-D (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-E (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-F (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-G (links | edit)