Search on: MULTIPLE ACYL COENZYME A DEHYDROGENASE DEFICIENCY 
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Descriptor English:   Multiple Acyl Coenzyme A Dehydrogenase Deficiency 
Descriptor Spanish:   Deficiencia Múltiple de Acyl Coenzima A Deshidrogenasa 
Descriptor Portuguese:   Deficiência Múltipla de Acil Coenzima A Desidrogenase 
Tree Number:   C16.320.565.100.614
C18.452.648.100.614
C18.452.660.612
Definition English:   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). 
History Note English:   2008 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
urine ultrasonography
veterinary virology
Record Number:   52627 
Unique Identifier:   D054069 

Occurrence in VHL:
 

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