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1,201 Possible Causes for Acyl CoA, Sn Glycerol 3 Phosphate O Acyltransferase

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  • Influenza

    […] consequence and accumulation of tissue LCFA has recently been shown to initiate apoptosis via increased ceramide in a variety of cell types. 20 21 Another factor is that toxic acyl-CoA[adc.bmjjournals.com]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Medium Chain Acyl CoA Dehydrogenase Deficiency

    Medium chain acyl-CoA dehydrogenase (MCAD) deficiency is an uncommon medical condition characterized by a deficiency of medium chain acyl-CoA dehydrogenase.[symptoma.com] Deficiency Medium-Chain Acyl-CoA Dehydrogenase Deficiency ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF; ACADMD ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF[wikidata.org] This drug should be omitted in the treatment of seizures in patients with possible medium chain acyl-CoA dehydrogenase deficiency.[ncbi.nlm.nih.gov]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Short Chain Acyl CoA Dehydrogenase Deficiency

    Short chain acyl CoA dehydrogenase deficiency is a rare genetic disorder that causes impaired utilization of energy from fat through fatty acid oxidation.[symptoma.com] Crystal structure of rat short chain acyl-CoA dehydrogenase complexed with acetoacetyl-CoA: comparison with other acyl-CoA dehydrogenases.[ncbi.nlm.nih.gov] Etiology Symptomatic SCAD deficiency is due to mutations in the acyl-CoA dehydrogenase, C-2 to C-3 short chain ACADS gene (12q24.31) as well as additional as yet unidentified[orpha.net]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • 2-Methylbutyryl-CoA Dehydrogenase Deficiency

    , and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism.[ghr.nlm.nih.gov] […] dehydrogenase deficiency or short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) is caused by a defect in the degradation pathway of the amino acid L-isoleucine[doi.org] CoA dehydrogenase deficiency E71.311 Medium chain acyl CoA dehydrogenase deficiency E71.312 Short chain acyl CoA dehydrogenase deficiency E71.313 Glutaric aciduria type II[icd10data.com]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Glutaric Aciduria Type 2

    The authors present a novel case of late-onset multiple acyl-CoA dehydrogenase deficiency showing varying responsivity to riboflavin treatment.[medlink.com] Cardiomyopathy and leukodystrophy are life-threatening complications of multiple acyl-CoA dehydrogenase deficiency (MADD).[ncbi.nlm.nih.gov] Multiple acyl-CoA dehydrogenase deficiency- (MADD-), also called glutaric aciduria type 2, associated leukodystrophy may be severe and progressive despite conventional treatment[ncbi.nlm.nih.gov]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Long Chain Hydroxyacyl-CoA Dehydrogenase Deficiency

    […] dehydrogenase deficiency (LCHAD), Long chain/very long chain acyl CoA dehydrogenase deficiency, Medium chain acyl CoA dehydrogenase deficiency (MCAD), Short chain acyl CoA[genedx.com] Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD).[pediatricfocus.wordpress.com] Abstract BACKGROUND Long chain 3-hydroxy-acyl-CoA dehydrogenase (LCHAD) is one of the enzymes involved in the breakdown of fatty acids.[bjo.bmj.com]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Carnitine Transporter Deficiency

    Differential diagnosis Differential diagnoses include other fat oxidation defects such as medium chain acyl-CoA dehydrogenase deficiency and very long chain acyl-CoA dehydrogenase[orpha.net] However, all of these patients were subsequently found to have medium-chain acyl-CoA dehydrogenase deficiency.[medlink.com] […] synthetases convert the fatty acids to fatty acyl-CoA .[pharmaxchange.info]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Mitochondrial Trifunctional Protein Deficiency

    Online: 28 April 2016 Part of the JIMD Reports book series (JIMD, volume 31) Abstract Deficiency of the mitochondrial trifunctional protein (TFP) and long-chain 3-Hydroxy Acyl-CoA[link.springer.com] […] dehydrogenase deficiency (LCHAD), Long chain/very long chain acyl CoA dehydrogenase deficiency, Medium chain acyl CoA dehydrogenase deficiency (MCAD), Short chain acyl CoA[genedx.com] Schematic demonstrating mitochondrial fatty acid beta-oxidation and effects of long-chain acyl CoA dehydrogenase deficiency (LCHAD) deficiency.[emedicine.com]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Peroxisomal Disease

    Term Name: peroxisomal acyl-CoA oxidase deficiency Search Ontology: Synonyms: Peroxisomal acyl-coenzyme A oxidase Definition: A peroxisomal disease that is characterized by[zfin.org] Google Scholar Suzuki Y, Mizue I, Kamei A, et al (2002) Peroxisomal acyl-CoA oxidase deficiency. J Pediatr 140 (1): 128-130.[link.springer.com] […] oxidase deficiency PAGES GENES INVOLVED Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID ACOX1 acox1 Peroxisomal acyl-CoA oxidase deficiency 264470 ZEBRAFISH MODELS[zfin.org]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase
  • Carnitine Deficiency

    Deficiency Medium-Chain Acyl-CoA Dehydrogenase Deficiency ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF; ACADMD ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF[wikidata.org] At least 3 separate acyl-CoA dehydrogenases are known; they are as follows: Long-chain acyl-CoA dehydrogenase (Length of fatty acid greater than C12) Medium-chain acyl CoA[emedicine.com] Abstract Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, one of the most common inherited metabolic disorders, is often mistaken for the sudden infant death syndrome[doi.org]

    Missing: Sn Glycerol 3 Phosphate O Acyltransferase

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