…Program Overview In partnership with Ionis Pharmaceuticals, this program provides genetic testing for familial chylomicronemia syndrome (FCS), a genetic condition which is characterized by high plasma triglyceride levels resulting from…

…panels. New Panels Bone Fragility and Fracture Disorders of Copper Metabolism Familial Chylomicronemia Familial Partial Lipodystrophy Galloway-Mowat Syndrome Generalized, Partial and Atypical Lipodystophy Hemolytic Anemia Medulloblastoma…

…to residents of the U.S. and Canada who meet testing eligibility criteria. The test must be ordered by a qualified healthcare provider. More Information Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) In partnership with Ionis…

…FILTERS NY Tests Only ORDER Test Kits # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Panels Familial Atrial Fibrillation Syndrome Panel Test Code Method Price 10323 Sequencing with CNV PGxome $990 Familial Chylomicronemia Panel Test…

…Calcification Disorders ENPP1 and ABCC6 Deficiencies ABCC6 Deficiency Only Genetic Testing Program for Amyotrophic Lateral Sclerosis (ALS) Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) Decode DEB Sponsored Testing Program…

…Calcification Disorders ENPP1 and ABCC6 Deficiencies ABCC6 Deficiency Only Genetic Testing Program for Amyotrophic Lateral Sclerosis (ALS) Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) Decode DEB Sponsored Testing Program…

…Calcification Disorders ENPP1 and ABCC6 Deficiencies ABCC6 Deficiency Only Genetic Testing Program for Amyotrophic Lateral Sclerosis (ALS) Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) Decode DEB Sponsored Testing Program…

…with CNV PGxome $990 Familial Chylomicronemia Panel Test Code Method Price 13025 Sequencing with CNV PGxome $990 Familial Cold Autoinflammatory Syndrome 2 via the NLRP12 Gene Test Code Method Price 11517 Sequencing with CNV PGxome $990 2067…

…via the APOA1 Gene Test Code Method Price 1403 Sanger Sequencing $580 8867 Sequencing with CNV PGxome $990 Familial Atrial Fibrillation Syndrome Panel Test Code Method Price 10323 Sequencing with CNV PGxome $990 Familial Chylomicronemia…

…Cholestasis Chylomicronemia Colorectal Cancer Congenital Anomalies of the Gastrointestinal Tract Congenital Diarrhea and Enteropathy Cystinuria Disorders of Fatty Acid Oxidation Familial Adenomatous Polyposis Gastric Cancer Glycogen Storage…

…Leukemia (AML) Anemia Bleeding Disorders Bone Marrow Failure Chylomicronemia Congenital Disorders of Glycosylation Crigler-Najjar Syndrome Diamond-Blackfan Anemia Factor VII Deficiency Fanconi Anemia Gilbert Syndrome Glucose-6-Phosphate…