Mobile Site ›

Print Friendly View

Unit Code 88830:
C5-OH Acylcarnitine, Quantitative, Urine

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.

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

Flow Injection Analysis-Tandem Mass Spectrometry (MS/MS)
Stable Isotope Dilution

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

C5-OH Acylcarnitine, QN, U

Ordering Mnemonic An alternate Mayo code (to the Unit Code) for a test

C5OHU

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

Soft-C5OHU