This test is not orderable.

Pheochromocytomas/Paraganglioma (PGL/PCC) Gene Panel

Synonyms	LAB1831 PHEO PGL SYNDROME PANEL PHEOCHROMOCYTOMAS, PARAGANGLIOMA SYNDROME PANEL
Cerner Name	PGL/PCC Panel
Clinical Info	A personal and/or family history of one or more paragangliomas or pheochromocytomas A pattern of cancer in which individuals with similar or related cancers (see table below) are on one side of the family and spanning multiple generations GeneDx code B395-5
Specimen Sources	Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous
Specimen Types	Blood
Specimen Volume	2 - 5 mL whole blood
Container	Lavender Top Tube
Collection Instructions	Container/Tube: Lavender top tube Specimen: 2 - 5 mL whole blood Transport Temperature: Room Temperature TAT: 4 Weeks
Transport Instructions	Room Temperature
Specimen Stability
Methodology	Deletion/Duplication Analysis Next-Gen Sequencing
Days Performed
Performing Laboratory	GeneDx
CPT	81403 81404 81405
PDM	1659877
Only Orderable at Locations:	Orderable Everywhere
Results
Result Interpretation See Report Includes Genes: FH, MAX, MEN1, NF1, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127, VHL
Forms	Hereditary Cancer Testing Requisition

LAB1831

Synonyms