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Test ID: C5OHU
C5-OH Acylcarnitine, Quantitative, Urine

Secondary ID A test code used for billing and in test definitions created prior to November 2011

88830

Useful For Suggests clinical disorders or settings where the test may be helpful

Evaluation of patients with an abnormal newborn screen showing elevations of C5-OH

Genetics Test Information Provides information that may help with selection of the correct test or proper submission of the test request

Evaluation of patients with an abnormal newborn screen showing elevations of C5-OH. The results are not informative when patient is receiving L-carnitine supplements.

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

Method Name A short description of the method used to perform the test

FLow Injection Analysis-Tandem Mass Spectrometry (FIA-MS/MS)

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

C5-OH Acylcarnitine, QN, U

Aliases Lists additional common names for a test, as an aid in searching

3-Hydroxy isovalerylcarnitine
3-Methylcrotonyl-CoA carboxylase deficiency
3-Methylcrotonylglycinuria
3-Methylglutaconic aciduria I
3-Methylglutaconic aciduria type 1
3-Methylglutaconic aciduria type I
3-Methylglutaconyl-CoA hydratase deficiency
3MCC
Acylcarnitines, urine
Beta-ketothiolase
Beta-ketothiolase deficiency
Biotinidase
Biotinidase deficiency
BKT
GA 1
GA I
GA1
GAI
Glutarylcarnitine
HCS
HCS deficiency
HMG-CoA (hydroxymethylglutaryl-CoA) lyase deficiency
Holocarboxylase deficiency
Holocarboxylase synthetase deficiency
Hydroxymethylglutaryl-CoA (HMG-CoA) Lyase Deficiency
MCC
MHBD
Multiple Carboxylase Deficiency