Correlagen Diagnostics Logo
Upper Lower Corner Blank Image Upper Right Corner
Blank Image
 

Test Menu (by Medical Subspecialty)

To order or for more information, please click on gene name.



Cardiology (to order or for more information, please click on gene name)

DSC2 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C)
DSG2 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C)
DSP Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C)
PKP2 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C)
TMEM43 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C)
NKX2-5 Atrial Septal Defect with Atrioventricular Block
APOB* Familial Hypercholesterolemia/Early-Onset Coronary Heart Disease
LDLR Familial Hypercholesterolemia/Early-Onset Coronary Heart Disease
PCSK9 Familial Hypercholesterolemia/Early-Onset Coronary Heart Disease
FBN1 Marfan Syndrome
ACTC Dilated Cardiomyopathy (DCM)
MYBPC3 Dilated Cardiomyopathy (DCM)
MYH7 Dilated Cardiomyopathy (DCM)
LMNA Dilated Cardiomyopathy (DCM)
TNNI3 Dilated Cardiomyopathy (DCM)
TNNT2 Dilated Cardiomyopathy (DCM)
TPM1 Dilated Cardiomyopathy (DCM)
ACTC Hypertrophic Cardiomyopathy (HCM)
MYBPC3 Hypertrophic Cardiomyopathy (HCM)
MYH7 Hypertrophic Cardiomyopathy (HCM)
MYL2 Hypertrophic Cardiomyopathy (HCM)
MYL3 Hypertrophic Cardiomyopathy (HCM)
LAMP2 Hypertrophic Cardiomyopathy (HCM)
PRKAG2 Hypertrophic Cardiomyopathy (HCM)
TNNI3 (cTnI) Hypertrophic Cardiomyopathy (HCM)
TNNT2 (cTnT) Hypertrophic Cardiomyopathy (HCM)
TPM1 Hypertrophic Cardiomyopathy (HCM)
TGFBR1 Loeys-Dietz Syndrome (LDS)
TGFBR2 Loeys-Dietz Syndrome (LDS)
PTPN11 Pulmonic Stenosis
TTR Transthyretin Amyloidosis
   
*Single Exon Sequencing  

Gasteroenterology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
CFTR Chronic Pancreatitis
PRSS1 Chronic Pancreatitis
SPINK1 Chronic Pancreatitis

Hematology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
HBB Beta Thalassemia

Immunology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
 
Overview Figure: Monogenic Causes of Immune Disorders
BTK Agammaglobulinemia (XLA)
AIRE Autoimmune disease or chronic mucocutaneous candidiasis (CMC)
TNFRSF13B (TACI) Common Variable Immunodeficiency (CVID)
CYBB Chronic Granulomatous Disease (CGD)
MEFV Familial Mediterranean Fever
STAT3 Hyper IgE Syndrome (HIES)
CD40LG Hyper IgM Syndrome (HIGM1)
AICDA Hyper IgM Syndrome (HIGM2)
CD40 Hyper IgM Syndrome (HIGM3)
UNG Hyper IgM Syndrome (HIGM5)
IKBKG (NEMO) Hypohydrotic Ectodermal Dysplasia with Immune Deficiency (HED-ID)
IFNGR1 Interferon Gamma Receptor Deficiency
IFNGR2 Interferon Gamma Receptor Deficiency
ADA Severe Combined Immunodeficiency (SCID)
CD3D Severe Combined Immunodeficiency (SCID)
CD3E Severe Combined Immunodeficiency (SCID)
DCLRE1C (ARTEMIS) Severe Combined Immunodeficiency (SCID (RS-SCID or SCIDA), including Omenn Syndrome)
IL2RG Severe Combined Immunodeficiency (SCID)
IL7R Severe Combined Immunodeficiency (SCID, including Omenn Syndrome)
JAK3 Severe Combined Immunodeficiency (SCID)
RAG1 Severe Combined Immunodeficiency (SCID, including Omenn Syndrome)
RAG2 Severe Combined Immunodeficiency (SCID, including Omenn Syndrome)
ZAP70 Severe Combined Immunodeficiency (SCID)
WAS Wiskott-Aldrich Syndrome (WAS)
SH2D1A X-linked Lymphoproliferative Disease (XLP)

Metabolic (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
GALT Galactosemia
ATP7B Wilson's Disease

Nephrology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
TCF2 (HNF1B) Renal Cysts and Diabetes (RCAD) (renal cysts)
VHL Renal cell carcinoma

Oncology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
MLH1 Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
MSH2 Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
MSH6 Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
PMS2 Hereditary Nonpolyposis Colorectal Cancer (HNPCC)

Ophthalmology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
BBS1 Retinal Degeneration
BBS2 Retinal Degeneration
VHL Retinal Hemangioblastoma

Pulmonology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
CFTR Cystic Fibrosis

Urology (to order or for more information, please click on gene name)

Testing for these indications now occurs at a different LabCorp site. Please contact the testing site's client services at 800-345-4363 for more information.
   
CFTR Congenital Bilateral Absence of the Vas Deferens

 

 
Blank Image
Blank Image Lower Right Corner
 
Blank Image