Renal Cancer Panel
Test Catalog Information
Test Catalog Synonyms | |
EPIC Synonyms | |
Cerner Primary Mnemonic | Renal Cell Cancer Panel |
EPIC Display Name | Renal Cancer Panel |
Allscripts (AEHR) Order Name | Not Orderable |
Sunrise Clinical Manager (SCM) Order Name | Not Orderable |
EPIC Inpatient Orderable | Yes |
EPIC Outpatient Orderable | Yes |
Cerner Results |
Renal Cell Cancer Panel |
Clinical Info |
1) The family history is suggestive of a predisposition to renal cancer. Although VHL, MET, FLCN, FH, TSC1 and TSC2 are the genes that are the most often associated with classic forms of hereditary renal cancer, there are several other genes that cause an increased risk of renal cancer. The OncoGeneDx Renal Cancer panel includes analysis of these genes as well as 12 other genes affecting renal cancer risk. Thus, the OncoGeneDx Renal Cancer panel offers increased clinical sensitivity compared to testing only for the most commonly associated genes. Furthermore, panel testing is more cost effective than stepwise genetic testing (for example, ordering VHL testing followed by additional genetic testing, if negative). 2) The differential diagnosis includes various hereditary cancer syndromes. For example, if the family history consists of multiple types of cancer, such as renal cancer in addition to pancreatic cancer, this may be associated with a cancer syndrome such as VHL or Lynch syndrome. 3) Genetic testing has already been ordered due to a family history suggestive of a hereditary cancer predisposition and all results have been negative. OncoGeneDx Renal Cancer Panel includes genes whose role in cancer predisposition has been described recently in addition to genes associated with classic hereditary cancer syndromes. |
Specimen Type | |
Container |
Lavender Top Tube |
Collection Instructions |
Container/Tube: Lavender top tube |
Transport Instructions |
Room Temperature |
Specimen Stability | |
Methodology |
Exon Array CGH, Next-gen Sequencing |
Days Performed | |
Performing Laboratory |
GeneDx |
CPT |
81403 |
PDM |
1659884 |
Desired Epic Build Renal Cancer Panel
Cerner Primary Mnemonic: | Renal Cell Cancer Panel | ||||||
PDM | 1659884 | ||||||
Informatics - Workgroup | Molecular-send outs | ||||||
Synonyms * | |||||||
Display Name * | Renal Cancer Panel | ||||||
Order Entry Specimen Sources * | |||||||
Order Entry Specimen Types |
Blood
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Ordering info (EPIC SmartText) | 1) The family history is suggestive of a predisposition to renal cancer. Although VHL, MET, FLCN, FH, TSC1 and TSC2 are the genes that are the most often associated with classic forms of hereditary renal cancer, there are several other genes that cause an increased risk of renal cancer. The OncoGeneDx Renal Cancer panel includes analysis of these genes as well as 12 other genes affecting renal cancer risk. Thus, the OncoGeneDx Renal Cancer panel offers increased clinical sensitivity compared to testing only for the most commonly associated genes. Furthermore, panel testing is more cost effective than stepwise genetic testing (for example, ordering VHL testing followed by additional genetic testing, if negative). 2) The differential diagnosis includes various hereditary cancer syndromes. For example, if the family history consists of multiple types of cancer, such as renal cancer in addition to pancreatic cancer, this may be associated with a cancer syndrome such as VHL or Lynch syndrome. 3) Genetic testing has already been ordered due to a family history suggestive of a hereditary cancer predisposition and all results have been negative. OncoGeneDx Renal Cancer Panel includes genes whose role in cancer predisposition has been described recently in addition to genes associated with classic hereditary cancer syndromes. | ||||||
IP Orderable | Yes | ||||||
OP Orderable | Yes | ||||||
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Special History | No | ||||||
Build Comments | |||||||
Filter * | genetics | ||||||
Procedure Category Change | |||||||
Cerner Results
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Actual Epic build
Procedure Id | 155109 | ||||||||||||
Pdm | 1659884 | ||||||||||||
Order Display Name | Renal Cancer Panel | ||||||||||||
Procedure Name | RENAL CANCER PANEL | ||||||||||||
Procedure Master Number | LAB155109 | ||||||||||||
Short Procedure Name | RENAL CANCER PANEL | ||||||||||||
Category Code | 21.0 | ||||||||||||
Category Code Record Name | LAB MOLECULAR DIAGNOSTICS ORDERABLES | ||||||||||||
Synonyms | |||||||||||||
Clinically Active | Yes | ||||||||||||
Orderable | Yes | ||||||||||||
Performable | Yes | ||||||||||||
Filter Genomics | Generic Genomics Procedure | ||||||||||||
Reference Link Url | https://labs.northwell.edu/epic/test/155109 | ||||||||||||
Ordering Instructions | |||||||||||||
Default Specimen Type | Blood | ||||||||||||
Specimen Type Pick List | Blood | ||||||||||||
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Specimen Source Pick List | Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous | ||||||||||||
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Order Questions | ["3048500000"] | ||||||||||||
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Inpatient Order Questions | ["3048500000"] | ||||||||||||
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Edp Amb Order Specific Questions Record Name | NH IP PATIENT COMPLETED CONSENT | ||||||||||||
Edp Ip Order Specific Questions Record Name | NH IP PATIENT COMPLETED CONSENT | ||||||||||||
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Ip Orderable | 1 | ||||||||||||
Op Orderable | 1 | ||||||||||||
EPIC OP AOEs
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EPIC Components (results)
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