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DeCS
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Descriptor English:
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Multiple Acyl Coenzyme A Dehydrogenase Deficiency
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Descriptor Spanish:
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Deficiencia Múltiple de Acil Coenzima A Deshidrogenasa
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Descriptor Portuguese:
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Deficiência Múltipla de Acil Coenzima A Desidrogenase
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Tree Number:
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C16.320.565.100.614
C18.452.648.100.614
C18.452.660.612
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Definition English:
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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). |
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History Note English:
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2008
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Allowable Qualifiers English:
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Record Number:
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52627
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Unique Identifier:
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D054069
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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