- Authorized users can sign in to the Client Price Portal for detailed fee information.
- Clients without portal access can contact Customer Service 24 hours a day, seven days a week.
- Prospective clients should contact their Regional Manager. For assistance, contact Customer Service.
This test has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.
82013-Acetylcholinesterase (if appropriate)
|Test ID||Test Order Name||Order LOINC Code|
|AFPA||Alpha-Fetoprotein, Amniotic Fluid||In Process|
|Result ID||Test Result Name||Result LOINC Code|
|DAT15||EDD by US Scan||11781-2|
|6740||Last Menstrual Period (LMP)||8665-2|
|24233||EDD by LMP||11779-6|
|24239||GA at Collection by Scan||11888-5|
|24240||GA at Collection by Dates||11885-1|
|9950||Alpha Fetoprotein, AF||43798-8|
|24237||Follow up||No LOINC Needed|
|24238||General Test Info||48767-8|
LOINC and CPT codes are provided by the performing laboratory.