Structured Summary
Abstract
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).
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Classification
Broader headings
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MeSH Record
Synonyms
32 entry terms
- Electron Transfer Flavoprotein Deficiency
- Ethylmalonic-Adipic Aciduria
- Ethylmalonic-Adipicaciduria
- Glutaric Acidemia Type II
- Glutaric Acidemia, Type 2
- Glutaric Aciduria II
- Glutaric Aciduria Type 2
- Glutaric Aciduria Type II
- Glutaric Aciduria, Type 2
- MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)
- Multiple Acyl-CoA Dehydrogenase Deficiency
- Multiple FAD Dehydrogenase Deficiency
- Aciduria, Ethylmalonic-Adipic
- Acidurias, Ethylmalonic-Adipic
- Ethylmalonic Adipic Aciduria
- Ethylmalonic Adipicaciduria
- Ethylmalonic-Adipic Acidurias
- MADD (Multiple Acyl CoA Dehydrogenase Deficiency)
- MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency)
- Multiple Acyl CoA Dehydrogenase Deficiency
- ETFA Deficiency
- ETFB Deficiency
- ETFDH Deficiency
- Electron Transfer Flavoprotein Alpha Subunit Deficiency
- Electron Transfer Flavoprotein Beta Subunit Deficiency
- Electron Transfer Flavoprotein Dehydrogenase Deficiency
- Glutaric Aciduria IIA
- Glutaric Aciduria IIB
- Glutaric Aciduria IIC
- ETFA Deficiencies
- ETFB Deficiencies
- ETFDH Deficiencies
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2008
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Multiple Acyl Coenzyme A Dehydrogenase Deficiency. Medical Subject Headings (MeSH). 2026. Unique ID D054069. http://id.nlm.nih.gov/mesh/2026/D054069
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency. In: Wikipedia. https://en.wikipedia.org/wiki/Glutaric_acidemia_type_2
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency. In: Wikidata. https://www.wikidata.org/wiki/Q1403045