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: http://www.knightdxlabs.com/home/methodological-test-listing?q=Molecular+Genetics
Affiliated with:
- OHSU Knight Cancer Institute, http://www.OHSUknightcancer.com/

This is one of your preferred labs. Add to preferred labs, See all preferred labs

GTR Lab ID: 1123, Last updated:2023-06-23

Personnel

Director: Stephen Moore, PhD, Lab Director
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

339 conditions/phenotypes with 139 tests
Enter text to narrow down the list

3-methylcrotonyl-CoA carboxylase 1 deficiency1 test
3-methylcrotonyl-CoA carboxylase 2 deficiency1 test
Aarskog syndrome1 test
Abetalipoproteinaemia1 test
Achondroplasia1 test
Achromatopsia1 test
Acquired long QT syndrome1 test
Acrocallosal syndrome1 test
Agenesis of the corpus callosum and congenital lymphedema1 test
Agenesis of the corpus callosum with peripheral neuropathy1 test
Alagille syndrome due to a JAG1 point mutation2 tests
Alagille syndrome due to a NOTCH2 point mutation2 tests
Alagille syndrome, ATP8B1 related1 test
Alzheimer disease1 test
Amyotrophic lateral sclerosis2 tests
Amyotrophic lateral sclerosis type 11 test
Amyotrophic lateral sclerosis type 101 test
Amyotrophic lateral sclerosis type 111 test
Amyotrophic lateral sclerosis type 121 test
Amyotrophic lateral sclerosis type 151 test
Amyotrophic lateral sclerosis type 181 test
Amyotrophic lateral sclerosis type 2, juvenile1 test
Amyotrophic lateral sclerosis type 41 test
Amyotrophic lateral sclerosis type 61 test
Amyotrophic lateral sclerosis type 91 test
Angelman syndrome4 tests
Angelman syndrome-like1 test
Antley-Bixler syndrome1 test
Aortic aneurysm1 test
Aplastic anemia1 test
Arginase deficiency1 test
Arrhythmogenic right ventricular cardiomyopathy3 tests
Arteriohepatic dysplasia1 test
Ataxia-telangiectasia-like disorder 11 test
Atrial fibrillation1 test
Autosomal dominant aplasia and myelodysplasia1 test
Autosomal recessive infantile epilepsy1 test
Autosomal recessive nonsyndromic hearing loss 1A1 test
Autosomal recessive Parkinson disease 143 tests
Autosomal recessive primary microcephaly2 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
Brugada syndrome3 tests
CARASIL syndrome1 test
Carcinoma of colon12 tests
Cardiac arrhythmia1 test
Cardiofaciocutaneous syndrome 11 test
Cardiomyopathy1 test
Carney complex1 test
Carnitine palmitoyl transferase 1A deficiency1 test
Carnitine palmitoyltransferase I deficiency , muscle1 test
Carnitine palmitoyltransferase II deficiency1 test
Catecholaminergic polymorphic ventricular tachycardia2 tests
Catecholaminergic polymorphic ventricular tachycardia 41 test
Central core myopathy1 test
Centronuclear myopathy1 test
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
Charcot-Marie-Tooth disease1 test
Charcot-Marie-Tooth disease X-linked dominant 11 test
Cholestasis, progressive familial intrahepatic, 41 test
Cholestasis, progressive familial intrahepatic, 51 test
Ciliopathy2 tests
Citrin deficiency2 tests
Colorectal cancer, hereditary nonpolyposis, type 25 tests
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency1 test
Congenital bile acid synthesis defect 21 test
Congenital cerebellar hypoplasia1 test
Congenital disorder of glycosylation1 test
Congenital muscular dystrophy1 test
Congenital muscular dystrophy due to LMNA mutation2 tests
Congenital myopathy1 test
Craniosynostosis syndrome1 test
Craniosynostosis-intellectual disability syndrome of 51N and Gettig1 test
Crouzon syndrome1 test
Cystic fibrosis4 tests
Developmental and epileptic encephalopathy, 21 test
Diamond-Blackfan anemia1 test
Dilated cardiomyopathy 3B1 test
Disorder of fatty acid metabolism1 test
Disorder of the urea cycle metabolism1 test
Dyskeratosis congenita1 test
Dyssynergia1 test
Dystonia 121 test
Dystonic disorder2 tests
Early-onset autosomal dominant Alzheimer disease1 test
Ehlers-Danlos syndrome2 tests
Ellis-van Creveld syndrome1 test
Emery-Dreifuss muscular dystrophy1 test
Endometrial carcinoma1 test
Epilepsy1 test
Episodic kinesigenic dyskinesia 11 test
Fabry disease2 tests
Familial adenomatous polyposis 12 tests
Familial adenomatous polyposis 21 test
Familial amyloid neuropathy1 test
Familial aortopathy2 tests
Familial aplasia of the vermis2 tests
Familial cancer of breast2 tests
Familial colorectal cancer14 tests
Familial hemiplegic migraine1 test
Familial hypercholesterolemia1 test
Familial hyperinsulinism2 tests
Familial medullary thyroid carcinoma2 tests
Familial multiple polyposis syndrome3 tests
Familial ovarian carcinoma1 test
Familial pancreatic carcinoma1 test
Familial restrictive cardiomyopathy2 tests
Familial thoracic aortic aneurysm and aortic dissection1 test
Fanconi anemia3 tests
Fanconi anemia complementation group A3 tests
Fanconi anemia complementation group B1 test
Fanconi anemia complementation group C2 tests
Fanconi anemia complementation group D11 test
Fanconi anemia complementation group D21 test
Fanconi anemia complementation group E2 tests
Fanconi anemia complementation group F2 tests
Fanconi anemia complementation group G2 tests
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
Frontotemporal dementia and/or amyotrophic lateral sclerosis 71 test
Fructose-biphosphatase deficiency1 test
Gastrointestinal stromal tumor1 test
Generalized epilepsy2 tests
Generalized juvenile polyposis/juvenile polyposis coli3 tests
Glanzmann thrombasthenia1 test
Gorlin syndrome1 test
Hemochromatosis type 12 tests
Hereditary breast ovarian cancer syndrome1 test
Hereditary cancer-predisposing syndrome2 tests
Hereditary disease5 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
Holoprosencephaly 111 test
Holoprosencephaly sequence2 tests
Hunter-McAlpine craniosynostosis1 test
Huntington disease1 test
Hyperalphalipoproteinemia 11 test
Hypercholesterolemia, familial, 11 test
Hyperlipidemia, familial combined, LPL related1 test
Hyperlipoproteinemia1 test
Hyperthyroidism1 test
Hypertriglyceridemia 11 test
Hypoalphalipoproteinemia, primary, 12 tests
Hypobetalipoproteinemia1 test
Hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism1 test
Idiopathic generalized epilepsy1 test
Inborn disorder of bile acid synthesis1 test
Infantile neuroaxonal dystrophy2 tests
Infantile seizures1 test
Inherited blood coagulation disorder1 test
Intellectual disability5 tests
Intellectual disability, CASK-related, X-linked1 test
Jackson-Weiss syndrome1 test
Joubert syndrome 11 test
Joubert syndrome 102 tests
Joubert syndrome 111 test
Joubert syndrome 121 test
Joubert syndrome 132 tests
Joubert syndrome 142 tests
Joubert syndrome 151 test
Joubert syndrome 162 tests
Joubert syndrome 172 tests
Joubert syndrome 181 test
Joubert syndrome 191 test
Joubert syndrome 22 tests
Joubert syndrome 211 test
Joubert syndrome 221 test
Joubert syndrome 231 test
Joubert syndrome 241 test
Joubert syndrome 251 test
Joubert syndrome 32 tests
Joubert syndrome 52 tests
Joubert syndrome 62 tests
Joubert syndrome 72 tests
Joubert syndrome 82 tests
Joubert syndrome 92 tests
Joubert syndrome and related disorders2 tests
Joubert syndrome with renal defect2 tests
Juvenile myoclonic epilepsy1 test
Lambotte syndrome1 test
Leber congenital amaurosis1 test
Left ventricular noncompaction1 test
Left ventricular noncompaction cardiomyopathy1 test
Li-Fraumeni syndrome1 test
Liddle syndrome 11 test
Limb-girdle muscular dystrophy2 tests
Lissencephaly1 test
Loeys-Dietz syndrome2 tests
Long QT syndrome3 tests
Lown-Ganong-Levine syndrome1 test
Lynch syndrome13 tests
Lynch syndrome 14 tests
Macrocephaly3 tests
Marfan syndrome3 tests
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections1 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
Methylcrotonyl-CoA carboxylase deficiency1 test
Microcephaly 16, primary, autosomal recessive1 test
Microcephaly 17, primary, autosomal recessive1 test
Microcephaly, cortical malformations, and intellectual disability1 test
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome1 test
Mitochondrial complex I deficiency1 test
Mitochondrial complex II deficiency, nuclear type 11 test
Mitochondrial complex III deficiency nuclear type 11 test
Mitochondrial disease1 test
Mitochondrial DNA Deletion Syndromes1 test
Mitochondrial trifunctional protein deficiency1 test
Muenke syndrome1 test
Multiple endocrine neoplasia type 41 test
Multiple endocrine neoplasia, type 11 test
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA2 tests
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB2 tests
Muscular dystrophy1 test
Myelodysplastic syndrome1 test
Nemaline myopathy2 tests
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
Neuromuscular disease4 tests
Neuronopathy, distal hereditary motor, type 5A1 test
Noonan syndrome2 tests
Noonan syndrome 11 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
Pheochromocytoma2 tests
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
Primary familial dilated cardiomyopathy3 tests
Primary familial hypertrophic cardiomyopathy3 tests
Progressive external ophthalmoplegia1 test
Progressive familial intrahepatic cholestasis type 12 tests
Progressive familial intrahepatic cholestasis type 31 test
Propionic acidemia1 test
PTEN hamartoma tumor syndrome1 test
Renal dysplasia and retinal aplasia1 test
Retinitis pigmentosa1 test
Retinitis pigmentosa 641 test
Rett syndrome3 tests
Rett syndrome, congenital variant2 tests
Saethre-Chotzen syndrome1 test
Schizencephaly1 test
SCOTT SYNDROME1 test
Seizure4 tests
Seizures, benign familial infantile, 21 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
Septo-optic dysplasia sequence1 test
Severe myoclonic epilepsy in infancy1 test
Short QT syndrome3 tests
Shprintzen-Goldberg syndrome3 tests
Shwachman-Diamond syndrome 11 test
Sitosterolemia2 tests
Steinert myotonic dystrophy syndrome1 test
Syndromic X-linked intellectual disability Lubs type1 test
Syndromic X-linked intellectual disability Najm type1 test
Tangier disease1 test
Thakker-Donnai syndrome1 test
Thrombocytopenia1 test
Thrombophilia due to activated protein C resistance1 test
Thrombophilia due to thrombin defect1 test
Thromboxane synthetase deficiency1 test
Torsades de pointes1 test
Torsion dystonia 21 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
Ventricular tachycardia2 tests
Visceral heterotaxy2 tests
Von Hippel-Lindau syndrome3 tests
West syndrome1 test
Wilson disease1 test
X-linked complicated corpus callosum dysgenesis1 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: 2023-12-31
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.