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Results 1 - 10 of 15 for "Acyl-CoA" dehydrogenase 9 deficiency
  1. ACAD9 deficiency 
    ... not show signs and symptoms of the condition. Acyl-CoA dehydrogenase 9 deficiency Deficiency of acyl-CoA dehydrogenase family member 9 ... deficiency due to ACAD9 deficiency Genetic Testing Registry: Acyl-CoA dehydrogenase 9 deficiency Isolated complex I deficiency National Organization for Rare ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  2. ACADM gene 
    ... Angel L, Andresen BS, Wilcken B. Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. Mol Genet Metab. 2006 Jan;87(1):32-9. doi: 10.1016/j.ymgme.2005.09.020. ...
    https://medlineplus.gov/genetics/gene/acadm - Genetics
  3. ACAD9 gene 
    ... MedlinePlus Genetics provides information about Mitochondrial complex I deficiency More About This Health Condition acyl-CoA dehydrogenase family member 9, mitochondrial acyl-Coenzyme A dehydrogenase family, member 9 ...
    https://medlineplus.gov/genetics/gene/acad9 - Genetics
  4. Mitochondrial trifunctional protein deficiency 
    ... control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency. Mol Genet Metab. 2007 Jan;90(1):64-9. doi: 10.1016/j.ymgme.2006.08.002. ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  5. Short-chain acyl-CoA dehydrogenase deficiency 
    ... J. Follow-up of patients with short-chain acyl-CoA dehydrogenase and isobutyryl-CoA dehydrogenase deficiencies identified through newborn screening: one center's experience. Genet Med. 2012 Mar;14(3):342-7. doi: 10.1038/gim.2011.9. Epub 2012 Jan 5. Citation on PubMed van ...
    https://medlineplus.gov/...t-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  6. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency. Mol Genet Metab. 2007 Jan;90(1):64-9. doi: 10.1016/j.ymgme.2006.08.002. ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  7. ACADS gene 
    ... variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level. Hum Genet. 2008 Aug;124(1):43-56. doi: 10.1007/s00439-008-0521-9. Epub 2008 Jun 4. Citation on PubMed Schmidt ...
    https://medlineplus.gov/genetics/gene/acads - Genetics
  8. 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase. Mol ... deficiency: clinical, biochemical, and pathological studies on three subjects ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  9. Glutaric acidemia type II 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov ... and acute life-threatening events in patients with glutaric acidemia type II. Mol Genet Metab. 2008 Jan;93(1):36-9. doi: 10.1016/j.ymgme.2007.09.015. ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-ii - Genetics
  10. HADH gene 
    ... mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase. Mol ... dehydrogenase deficiency reveals the importance of beta-oxidation in insulin ...
    https://medlineplus.gov/genetics/gene/hadh - Genetics
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