Atypical hemolytic uremic syndrome susceptibility and related disorders Deletion/ Duplication panel
- GTR Test IDHelpEach Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. When a laboratory updates a registered test, a new version number is assigned.: GTR000592214.1
- Last updated: 2020-11-30
- Test version history
- 592214.1, last updated: 2020-11-30
Clinical testHelpIn the U.S., clinical tests must be performed under CLIA certification. When a lab uses the same methods for a test in both clinical and research settings, the test appears as two separate GTR records. for Atypical hemolytic-uremic syndrome
Offered by HNL Genomics Connective Tissue Gene Tests
Overview
Test name
HelpThe name the laboratory assigns the test. Used as the default title of the page specific to the test.Atypical hemolytic uremic syndrome susceptibility and related disorders Deletion/ Duplication panel
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Diagnosis, Mutation Confirmation
Click Indication tab for more information.
Please use the equisition form and easy-to-use submission instructions available on the CTGT web site
Order URL HelpLink to the laboratory webpage with information about how to order this test. Please note that clicking on this link will open a new tab in your internet browser.: http://ctgt.net/how-to-order
Specimen source
Methodology
HelpThe assay's major method category (biochemical, cytogenetic or molecular genetics); method category (i.e. enzyme assay, chromosome breakage studies, targeted mutation analysis); methodology (i.e. the name of the method used) and instruments used when performing this test.- Molecular Genetics
- DDeletion/duplication analysis
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
- CSequence analysis of the entire coding region
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
Clinical validity
HelpHow consistently and accurately the test detects or predicts the intermediate or final outcomes of interest. Lab-provided.Not provided
Test services
HelpLaboratory's order or catalog code for the test (used in the order requisition form).- Clinical Testing/Confirmation of Mutations Identified Previously, Order code: 5146
- Confirmation of research findings
- Custom Prenatal Testing, commentsOptional Maternal Cell Contamination (MCC) testing is available for all prenatal tests
- Custom mutation-specific/Carrier testing
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