Diseases

Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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).

National Library of MedicineMedical Subject Headings2026

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).

MeSH Record

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

Tree Numbers

  1. C16w.320w.565w.100.614w
  2. C18.452w.648w.100.614w
  3. C18.452w.660w.612w

AMA Style

References

  1. 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
  2. Multiple Acyl Coenzyme A Dehydrogenase Deficiency. In: Wikipedia. https://en.wikipedia.org/wiki/Glutaric_acidemia_type_2
  3. Multiple Acyl Coenzyme A Dehydrogenase Deficiency. In: Wikidata. https://www.wikidata.org/wiki/Q1403045