Correlagen Subspecialties

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	Early-Onset Coronary Heart Disease
LDLR	Early-Onset Coronary Heart Disease
PCSK9	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

Endocrinology

Correlagen has exclusively licensed its endocrine and metabolic testing for physician-authorized or physician-ordered diagnostic or prognostic use in the US, Canada, and Japan to Athena Diagnostics, Inc. Please click here for a detailed list of tests available for endocrine and metabolic indications and to order any of the tests.

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

CFTR	Chronic Pancreatitis
PRSS1	Chronic Pancreatitis
SPINK1	Chronic Pancreatitis

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

HBB	Beta Thalassemia

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

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)

GALT	Galactosemia
ATP7B	Wilson's Disease

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

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)

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)

BBS1	Retinal Degeneration
BBS2	Retinal Degeneration
VHL	Retinal Hemangioblastoma

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

CFTR	Cystic Fibrosis

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

CFTR	Congenital Bilateral Absence of the Vas Deferens