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
|
| 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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2020 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" by people in Profiles.
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Tolomeo M, Chimienti G, Lanza M, Barbaro R, Nisco A, Latronico T, Leone P, Petrosillo G, Liuzzi GM, Ryder B, Inbar-Feigenberg M, Colella M, Lezza AMS, Olsen RKJ, Barile M. Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2. Free Radic Res. 2022 Jul-Aug; 56(7-8):511-525.
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Tolomeo M, Nisco A, Leone P, Barile M. Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy. Int J Mol Sci. 2020 Jul 26; 21(15).