Multiple Acyl Coenzyme A Dehydrogenase Deficiency
"Multiple Acyl Coenzyme A Dehydrogenase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (AMINO ACIDS, BRANCHED-CHAIN); LYSINE; and CHOLINE catabolism, that is due to defects in either subunit of ELECTRON TRANSFER FLAVOPROTEIN or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1).
| Descriptor ID |
D054069
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| MeSH Number(s) |
C16.320.565.100.614 C18.452.648.100.614 C18.452.660.612
|
| Concept/Terms |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency- Multiple Acyl Coenzyme A Dehydrogenase Deficiency
- Ethylmalonic-Adipic Aciduria
- Aciduria, Ethylmalonic-Adipic
- Acidurias, Ethylmalonic-Adipic
- Ethylmalonic Adipic Aciduria
- Ethylmalonic-Adipic Acidurias
- Ethylmalonic-Adipicaciduria
- Ethylmalonic Adipicaciduria
- Glutaric Acidemia Type II
- Glutaric Acidemia, Type 2
- Glutaric Aciduria II
- Glutaric Aciduria Type II
- Glutaric Aciduria, Type 2
- MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)
- MADD (Multiple Acyl CoA Dehydrogenase Deficiency)
- MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency)
- Multiple Acyl-CoA Dehydrogenase Deficiency
- Multiple Acyl CoA Dehydrogenase Deficiency
- Multiple FAD Dehydrogenase Deficiency
- Electron Transfer Flavoprotein Deficiency
- Glutaric Aciduria Type 2
Glutaric Aciduria IIC- Glutaric Aciduria IIC
- ETFDH Deficiency
- ETFDH Deficiencies
- Electron Transfer Flavoprotein Dehydrogenase Deficiency
Glutaric Aciduria IIA- Glutaric Aciduria IIA
- ETFA Deficiency
- ETFA Deficiencies
- Electron Transfer Flavoprotein Alpha Subunit Deficiency
Glutaric Aciduria IIB- Glutaric Aciduria IIB
- Electron Transfer Flavoprotein Beta Subunit Deficiency
- ETFB Deficiency
- ETFB Deficiencies
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Below are MeSH descriptors whose meaning is more general than "Multiple Acyl Coenzyme A Dehydrogenase Deficiency".
Below are MeSH descriptors whose meaning is more specific than "Multiple Acyl Coenzyme A Dehydrogenase Deficiency".
This graph shows the total number of publications written about "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" by people in this website by year, and whether "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" was a major or minor topic of these publications.
Below are the most recent publications written about "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" by people in Profiles.
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Multiple acyl-CoA dehydrogenase deficiency kills Mycobacterium tuberculosis in vitro and during infection. Nat Commun. 2021 11 15; 12(1):6593.
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Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2. Am J Med Genet A. 2020 10; 182(10):2426-2431.
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Homozygous B4GALNT1 mutation and biochemical glutaric acidemia type II: A case report. Clin Neurol Neurosurg. 2020 02; 189:105553.
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Acquired multiple acyl-CoA dehydrogenase deficiency and marked selenium deficiency causing severe rhabdomyolysis in a horse. Can Vet J. 2015 Nov; 56(11):1166-71.
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Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases. Brain Dev. 2016 Mar; 38(3):293-301.
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Evidence for genetic heterogeneity in D-2-hydroxyglutaric aciduria. Hum Mutat. 2010 Mar; 31(3):279-83.