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Nume Disorders of fatty-acid metabolism
Pagina Web apps.who.int

Vezi şi

Boli A-Z 3-Hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Adrenoleukodystrophy Carnitine-Acylcarnitine Translocase Deficiency Carnitine Deficiency, Systemic Primary Carnitine Palmitoyltransferase I Deficiency Carnitine Palmitoyltransferase Ii Deficiency, Infantile Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal Carnitine Palmitoyltransferase Ii Deficiency, Myopathic, Stress-Induced D-Bifunctional Protein Deficiency Hyperinsulinism Due to Short Chain 3-Hydroxylacyl-Coa Dehydrogenase Deficiency Lipid Metabolism Disorder Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Mitochondrial Complex I Deficiency Due to Acad9 Deficiency Multiple Acyl-Coa Dehydrogenase Deficiency Neonatal Adrenoleukodystrophy Peroxisomal Acyl-Coa Oxidase Deficiency Peroxisomal Fatty Acyl-Coa Reductase 1 Disorder Succinyl-Coa:3-Oxoacid-Coa Transferase Deficiency Transient Neonatal Multiple Acyl-Coa Dehydrogenase Deficiency
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