Knight Diagnostic Laboratories - Molecular Diagnostic Center

Knight Diagnostic Laboratories - Molecular Diagnostic Center, KDL
Oregon Health & Science University (OHSU)
2525 SW 3rd Ave, Suite 350
Portland, Oregon, United States 97201
Phone: 855-535-1522
Fax: 855-535-1329
Email: kdlclientservices@ohsu.edu
Online Contact: http://www.knightdxlabs.com/
Website: https://knightdxlabs.ohsu.edu/
Affiliated with:
- OHSU Knight Cancer Institute, http://www.OHSUknightcancer.com/

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GTR Lab ID: 1123, Last updated:2024-10-24

Personnel

Director: Alaa Koleilat, PhD, FACMG, Lab Director
Phone: 503-494-5400
Director: Richard Press, PhD, MD, Lab Director
Phone: 503-494-5400
Fax: 503-494-6922
Email: pressr@ohsu.edu
Sarah McCabe, Laboratory Contact
Phone: 503-494-5400
Fax: 503-494-6922
Email: mccabe@ohsu.edu

Conditions and tests

201 conditions/phenotypes with 55 tests
Enter text to narrow down the list

Achondroplasia1 test
Alagille syndrome due to a JAG1 point mutation1 test
Alagille syndrome due to a NOTCH2 point mutation1 test
Alagille syndrome, ATP8B1 related1 test
Angelman syndrome2 tests
Angelman syndrome-like1 test
Antley-Bixler syndrome1 test
Aplastic anemia1 test
Arteriohepatic dysplasia1 test
Ataxia-telangiectasia-like disorder 11 test
Autosomal dominant aplasia and myelodysplasia1 test
Autosomal recessive nonsyndromic hearing loss 1A1 test
Autosomal recessive Parkinson disease 143 tests
Baller-Gerold syndrome1 test
Bardet-Biedl syndrome1 test
Basal cell carcinoma, susceptibility to, 11 test
Beare-Stevenson cutis gyrata syndrome1 test
Benign recurrent intrahepatic cholestasis type 11 test
Benign recurrent intrahepatic cholestasis type 21 test
Bernard-Soulier syndrome type C1 test
Bernard-Soulier syndrome, type A1 test
Bernard-Soulier syndrome, type A2, autosomal dominant1 test
Bernard-Soulier syndrome, type B1 test
Birt-Hogg-Dube syndrome1 test
Bloom syndrome1 test
Bone marrow failure syndrome 31 test
Breast neoplasm1 test
Breast-ovarian cancer, familial, susceptibility to, 11 test
Breast-ovarian cancer, familial, susceptibility to, 21 test
Carcinoma of colon1 test
Carney complex1 test
Carnitine palmitoyl transferase 1A deficiency1 test
Cholestasis, progressive familial intrahepatic, 41 test
Cholestasis, progressive familial intrahepatic, 51 test
Ciliopathy1 test
Citrin deficiency1 test
Colorectal cancer, hereditary nonpolyposis, type 21 test
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency1 test
Congenital bile acid synthesis defect 21 test
Craniosynostosis syndrome1 test
Craniosynostosis-intellectual disability syndrome of 51N and Gettig1 test
Crouzon syndrome1 test
Cystic fibrosis4 tests
Diamond-Blackfan anemia1 test
Dilated cardiomyopathy 3B1 test
Dyskeratosis congenita1 test
Ehlers-Danlos syndrome1 test
Ellis-van Creveld syndrome1 test
Endometrial carcinoma1 test
Fabry disease1 test
Familial adenomatous polyposis 11 test
Familial adenomatous polyposis 21 test
Familial aortopathy1 test
Familial aplasia of the vermis1 test
Familial cancer of breast2 tests
Familial colorectal cancer3 tests
Familial hyperinsulinism1 test
Familial medullary thyroid carcinoma2 tests
Familial multiple polyposis syndrome1 test
Familial ovarian carcinoma1 test
Familial pancreatic carcinoma1 test
Fanconi anemia2 tests
Fanconi anemia complementation group A1 test
Fanconi anemia complementation group B1 test
Fanconi anemia complementation group C1 test
Fanconi anemia complementation group D11 test
Fanconi anemia complementation group D21 test
Fanconi anemia complementation group E1 test
Fanconi anemia complementation group F1 test
Fanconi anemia complementation group G1 test
Fanconi anemia complementation group I1 test
Fanconi anemia complementation group J1 test
Fanconi anemia complementation group L1 test
Fanconi anemia complementation group N1 test
Fanconi anemia complementation group O1 test
Fanconi anemia complementation group P1 test
Fanconi anemia, complementation group M1 test
Focal segmental glomerulosclerosis 4, susceptibility to1 test
Fragile X syndrome1 test
Fragile X-associated tremor/ataxia syndrome1 test
Gastrointestinal stromal tumor1 test
Generalized juvenile polyposis/juvenile polyposis coli1 test
Glanzmann thrombasthenia1 test
Gorlin syndrome1 test
Hereditary breast ovarian cancer syndrome1 test
Hereditary cancer-predisposing syndrome2 tests
Hereditary hearing loss and deafness1 test
Hereditary leiomyomatosis and renal cell cancer1 test
Hereditary pancreatitis1 test
Hereditary spastic paraplegia 351 test
Hereditary von Willebrand disease1 test
Hermansky-Pudlak syndrome1 test
Heterotaxy, visceral, 1, X-linked1 test
Heterotaxy, visceral, 4, autosomal1 test
Hunter-McAlpine craniosynostosis1 test
Huntington disease1 test
Inborn disorder of bile acid synthesis1 test
Infantile neuroaxonal dystrophy2 tests
Inherited blood coagulation disorder1 test
Jackson-Weiss syndrome1 test
Joubert syndrome 101 test
Joubert syndrome 131 test
Joubert syndrome 141 test
Joubert syndrome 151 test
Joubert syndrome 161 test
Joubert syndrome 171 test
Joubert syndrome 21 test
Joubert syndrome 31 test
Joubert syndrome 51 test
Joubert syndrome 61 test
Joubert syndrome 71 test
Joubert syndrome 81 test
Joubert syndrome 91 test
Joubert syndrome with renal defect1 test
Leber congenital amaurosis1 test
Li-Fraumeni syndrome1 test
Liddle syndrome 11 test
Loeys-Dietz syndrome1 test
Lynch syndrome2 tests
Marfan syndrome1 test
Maturity-onset diabetes of the young type 11 test
Maturity-onset diabetes of the young type 101 test
Maturity-onset diabetes of the young type 111 test
Maturity-onset diabetes of the young type 131 test
Maturity-onset diabetes of the young type 141 test
Maturity-onset diabetes of the young type 21 test
Maturity-onset diabetes of the young type 31 test
Maturity-onset diabetes of the young type 41 test
Maturity-onset diabetes of the young type 61 test
Maturity-onset diabetes of the young type 71 test
Maturity-onset diabetes of the young type 81 test
Maturity-onset diabetes of the young type 91 test
McKusick-Kaufman syndrome1 test
Meckel-Gruber syndrome1 test
Melanoma, cutaneous malignant, susceptibility to, 21 test
Melanoma, cutaneous malignant, susceptibility to, 31 test
Melanoma, cutaneous malignant, susceptibility to, 81 test
Muenke syndrome1 test
Multiple endocrine neoplasia type 2A2 tests
Multiple endocrine neoplasia type 2B2 tests
Multiple endocrine neoplasia type 41 test
Multiple endocrine neoplasia, type 11 test
Myelodysplastic syndrome1 test
Nephronophthisis1 test
Nephronophthisis 121 test
Neurodegeneration with brain iron accumulation6 tests
Neurodegeneration with brain iron accumulation 2B3 tests
Neurodegeneration with brain iron accumulation 41 test
Neuroferritinopathy1 test
Neurofibromatosis-Noonan syndrome1 test
Noonan syndrome1 test
Oculocutaneous albinism type 71 test
Orofaciodigital syndrome1 test
Orofaciodigital syndrome I1 test
Ovarian cancer1 test
Pancytopenia-developmental delay syndrome1 test
Papillary renal cell carcinoma type 11 test
Paragangliomas 21 test
Parathyroid carcinoma1 test
Parkinson disease1 test
Pfeiffer syndrome1 test
Pheochromocytoma1 test
Pierre Robin syndrome-faciodigital anomaly syndrome1 test
Pigmentary pallidal degeneration1 test
PLA2G6-associated neurodegeneration3 tests
Platelet disorder, undefined1 test
Prader-Willi syndrome1 test
Premature ovarian failure1 test
Primary ciliary dyskinesia1 test
Progressive familial intrahepatic cholestasis type 11 test
Progressive familial intrahepatic cholestasis type 31 test
PTEN hamartoma tumor syndrome1 test
Renal dysplasia and retinal aplasia1 test
Retinitis pigmentosa1 test
Retinitis pigmentosa 641 test
Rett syndrome2 tests
Rett syndrome, congenital variant2 tests
Saethre-Chotzen syndrome1 test
SCOTT SYNDROME1 test
Senior-Loken syndrome 11 test
Senior-Loken syndrome 41 test
Senior-Loken syndrome 51 test
Senior-Loken syndrome 61 test
Senior-Loken syndrome 71 test
Shprintzen-Goldberg syndrome2 tests
Shwachman-Diamond syndrome 11 test
Steinert myotonic dystrophy syndrome1 test
Syndromic X-linked intellectual disability Lubs type1 test
Thrombocytopenia1 test
Thrombophilia due to activated protein C resistance1 test
Thrombophilia due to thrombin defect1 test
Thromboxane synthetase deficiency1 test
TWIST1-related craniosynostosis1 test
Urinary bladder carcinoma1 test
Usher syndrome type 1C1 test
Usher syndrome type 1G1 test
Usher syndrome type 21 test
Usher syndrome type 2A1 test
Visceral heterotaxy1 test
Von Hippel-Lindau syndrome2 tests
Wilson disease1 test

List of services

Clinical Testing/Confirmation of Mutations Identified Previously
Confirmation of research findings
Custom Balanced Chromosome Rearrangement Studies
Custom Deletion/Duplication Testing
Prenatal testing
Custom Sequence Analysis
Custom microarray analysis
Carrier testing
Insurance billing
Maternal cell contamination study (MCC)
Mutation Confirmation
Result interpretation

List of certifications/licenses

Certifications

CLIAHelpCertification number assigned by the Clinical Laboratory Improvement Amendments (CLIA) program to the laboratory director. Minimal field for US labs offering clinical tests. Optional field for international labs or US labs performing research tests. If pending renewal or record has not been updated, the expiration date may be in the past., Number: 38D0881787, Expiration date: 2025-12-31
CAP, Number: 2442619, Expiration date: 2025-06-15

Participation in external programs

Standardization programs

CETT Program (Collaboration Education and Test Translation)
Locus-specific Databases
Mutation-specific Databases

Data exchange Programs

CETT Program (Collaboration Education and Test Translation)
Locus-specific Databases
Mutation-specific Databases

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.