TRIMETHYLAMINURIA (FMO3) GENE SEQUENCING

A genetic test to detect mutations in the FMO3 gene, causing trimethylaminuria, a metabolic disorder that results in a strong body odor due to the accumulation of trimethylamine.

Also known asTrimethylaminuria (fmo3) Gene Sequencing Trimethylaminuria (fmo3) Gene Sequencing

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
TRIMETHYLAMINURIA (FMO3) GENE SEQUENCING includes 1 parameter

  • Specimen

Test code

G756

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Others (fx)Others2 ML

Specimen stability information

Others (Fx)

Specimen rejection criteria

Test run frequency

Every Day TIME - 10:00

Turn around time

28 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

TRIMETHYLAMINURIA (FMO3) GENE SEQUENCING

22000