John Welsh Cardiovascular Diagnostic Laboratory

Personnel

Director: Yuxin Fan, PhD, MD, FACMG, Lab Director
Phone: 832-824-4155
Fax: 832-825-5159
Email: [email protected]

Conditions and tests

55 conditions/phenotypes with 65 tests
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3-Methylglutaconic aciduria type 22 tests
Andersen Tawil syndrome1 test
Aortic aneurysm, familial thoracic 41 test
Aortic aneurysm, familial thoracic 61 test
Arrhythmogenic right ventricular cardiomyopathy1 test
Arrhythmogenic right ventricular dysplasia 11 test
Arrhythmogenic right ventricular dysplasia 101 test
Arrhythmogenic right ventricular dysplasia 111 test
Arrhythmogenic right ventricular dysplasia 121 test
Arrhythmogenic right ventricular dysplasia 21 test
Arrhythmogenic right ventricular dysplasia 51 test
Arrhythmogenic right ventricular dysplasia 81 test
Arrhythmogenic right ventricular dysplasia 91 test
Brugada syndrome3 tests
Brugada syndrome 11 test
Brugada syndrome 21 test
Brugada syndrome 31 test
Brugada syndrome 41 test
Brugada syndrome 51 test
Brugada syndrome 61 test
Brugada syndrome 71 test
Brugada syndrome 81 test
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 11 test
Catecholaminergic polymorphic ventricular tachycardia 21 test
Caveolinopathy1 test
Charcot-Marie-Tooth disease type 2B11 test
Danon disease1 test
Desmin-related myofibrillar myopathy1 test
Dilated cardiomyopathy 1A2 tests
Dilated cardiomyopathy 1C1 test
Dilated cardiomyopathy 1I2 tests
Ectopia lentis 1, isolated, autosomal dominant1 test
Emery-Dreifuss muscular dystrophy 2, autosomal dominant2 tests
Familial aortopathy1 test
Familial partial lipodystrophy, Dunnigan type1 test
Familial thoracic aortic aneurysm and aortic dissection3 tests
Holt-Oram syndrome1 test
Hutchinson-Gilford syndrome2 tests
Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome1 test
Isolated Nonsyndromic Congenital Heart Disease/Defects1 test
Leigh Syndrome (nuclear DNA mutation)1 test
Loeys-Dietz syndrome1 test
Loeys-Dietz syndrome 11 test
Loeys-Dietz syndrome 21 test
Long QT syndrome 91 test
Mandibuloacral dysplasia1 test
Marfan syndrome1 test
MASS syndrome1 test
Myofibrillar myopathy 41 test
Noncompaction of left ventricular myocardium, familial isolated1 test
Primary pulmonary hypertension1 test
Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia1 test
SUDDEN INFANT DEATH SYNDROME1 test
Telangiectasia, hereditary hemorrhagic, type 13 tests
X-linked Emery-Dreifuss muscular dystrophy1 test

List of services

Clinical Testing/Confirmation of Mutations Identified Previously

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: 45D0703562, Expiration date: 2025-02-08
CAP, Number: 2108401, Expiration date: 2023-09-30

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.