Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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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.

MeSH information

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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 Aciduria II Glutaric Aciduria Type II 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 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

Below are MeSH descriptors whose meaning is more general than "Multiple Acyl Coenzyme A Dehydrogenase Deficiency".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C16.320.565.100.614]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C18.452.648.100.614]
Mitochondrial Diseases [C18.452.660]
Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C18.452.660.612]

Below are MeSH descriptors whose meaning is related to "Multiple Acyl Coenzyme A Dehydrogenase Deficiency".

Below are MeSH descriptors whose meaning is more specific than "Multiple Acyl Coenzyme A Dehydrogenase Deficiency".

publications

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