 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
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| 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 |
|---|
| 2013 | 1 | 0 | 1 | | 2020 | 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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van Rijt WJ, Jager EA, Allersma DP, Aktuglu Zeybek A?, Bhattacharya K, Debray FG, Ellaway CJ, Gautschi M, Geraghty MT, Gil-Ortega D, Larson AA, Moore F, Morava E, Morris AA, Oishi K, Schiff M, Scholl-B?rgi S, Tchan MC, Vockley J, Witters P, Wortmann SB, van Spronsen F, Van Hove JLK, Derks TGJ. Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency. Genet Med. 2020 05; 22(5):908-916.
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Kim SH, Scott SA, Bennett MJ, Carson RP, Fessel J, Brown HA, Ess KC. Multi-organ abnormalities and mTORC1 activation in zebrafish model of multiple acyl-CoA dehydrogenase deficiency. PLoS Genet. 2013 Jun; 9(6):e1003563.
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