- ARUP Laboratories | National Reference Laboratory
ARUP provides reference laboratory testing for hospitals and health centers, serving the diagnostic needs of patients We also consult on lab management, utilization, and operations
- OSR Deidentified ANSRLTR - ARUP Lab
This test was developed and its performance characteristics determined by the University of Washington Department of Laboratory Medicine It has not been cleared or approved by the US Food and Drug Administration This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) as qualified to perform high complexity clinical laboratory testing This test is used for
- OSR Deidentified ANSRLTR
H=High, L=Low, *=Abnormal, C=Critical Patient: Patient, Example ARUP Accession: 24-341-114328 Patient Identifiers: 01234567890ABCD, 012345 Visit Number (FIN): 01234567890ABCD Page 2 of 2 | Printed: 1 17 2025 11:37:19 AM 4848
- OSR Deidentified ANSR - ARUP Lab
H=High, L=Low, *=Abnormal, C=Critical Patient: Patient, Example ARUP Accession: 23-037-112696 Patient Identifiers: 01234567890ABCD, 012345 Visit Number (FIN): 01234567890ABCD Page 1 of 2 | Printed: 2 7 2023 8:14:41 AM 4848
- ARUP Alumni Feature: Eric Konnick, MD, MS, Reflects on Journey From . . .
Eric Konnick, MD, MS, started his career as a scientist in ARUP’s Molecular Pathology Lab Now he’s the associate director of the Genetics and Solid Tumor Lab at the University of Washington Medical Center Learn how ARUP helped shape his career and how his work impacts both patients and the future of lab medicine
- Tasso and ARUP Laboratories Announce Partnership, Combined Offering for . . .
The partnership combines Tasso’s clinical grade blood collection solutions and ARUP’s gold standard testing capabilities to streamline and accelerate decentralized clinical research
- Contact Us - ARUP Laboratories
Client Services agents are available 24 hours per day:Phone: 1-800-522-2787Fax: 1-800-522-2706Email: clientservices@aruplab comSales InquiriesPlease complete this request form for sales-based questions and a local Account Executive will contact you
- Hereditary Hemorrhagic Telangiectasia Panel | Test Fact Sheet
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver, and brain Overlapping disorders include BMP9 GDF2-related vascular-anomaly syndrome, BMPR2-related disorders, capillary malformation-arteriovenous malformation (CM-AVM), and SMAD4
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