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HelpTest Code PBGU Porphobilinogen, Quantitative, Random, Urine
Additional Codes
| Mayo Test ID | COPIA Test code | EPIC Test Codes | |
|---|---|---|---|
| PBGU | PBGU-Porphobilinogen, Quantitative, Random, Urine | LAB1346 | PORPHOBILINOGEN, QUANT, URINE, RANDOM |
Reporting Name
Porphobilinogen, QN, Random, UUseful For
First-order test for evaluating a suspected acute porphyria: acute intermittent porphyria, hereditary coproporphyria, and variegate porphyria
Testing Algorithm
For more information see:
-The Heme Biosynthetic Pathway
Method Name
Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Specimen Type
UrineShipping Instructions
Ship specimen protected from light.
Necessary Information
Include a list of medications the patient is currently taking.
Specimen Required
Patient Preparation: Patient must not consume any alcohol for at least 24 hours prior to collection.
Supplies: Urine Container-Amber, 60 mL (T596)
Specimen Volume: 20 mL
Collection Instructions:
1. Collect a random urine specimen.
2. No preservative necessary but pH must be above 5.0.
3. Specimens should be protected from light and frozen immediately following collection.
Specimen Minimum Volume
15 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Urine | Frozen (preferred) | 7 days | LIGHT PROTECTED |
| Refrigerated | 7 days | LIGHT PROTECTED |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Special Instructions
Reference Values
≤1.3 mcmol/L
Day(s) Performed
Monday through Friday
CPT Code Information
84110
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| PBGU | Porphobilinogen, QN, Random, U | 2811-8 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 29365 | Porphobilinogen, U | 2811-8 |
| 29366 | Interpretation (PBGU) | 59462-2 |
| 35032 | Reviewed By | 18771-6 |
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.Report Available
2 to 4 daysForms
If not ordering electronically, complete, print, and send a Biochemical Genetics Test Request (T798) with the specimen.