…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…

…Panel Test Code Method Price 10323 Sequencing with CNV PGxome $990 Familial Chylomicronemia Panel Test Code Method Price 13025 Sequencing with CNV PGxome $990 Familial Hemiplegic Migraine and Alternating Hemiplegia of Childhood Panel Test…

…Panel Test Code Method Price 10323 Sequencing with CNV PGxome $990 Familial Chylomicronemia Panel Test Code Method Price 13025 Sequencing with CNV PGxome $990 Familial Hemiplegic Migraine and Alternating Hemiplegia of Childhood Panel Test…

…Program for Amyotrophic Lateral Sclerosis (ALS) Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) Decode DEB Sponsored Testing Program Movement Disorder Genetic Test Program No-Cost Genetic Testing Program for Cholestasis…

…Program for Amyotrophic Lateral Sclerosis (ALS) Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) Decode DEB Sponsored Testing Program Movement Disorder Genetic Test Program No-Cost Genetic Testing Program for Cholestasis…

…Program for Amyotrophic Lateral Sclerosis (ALS) Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) Decode DEB Sponsored Testing Program Movement Disorder Genetic Test Program No-Cost Genetic Testing Program for Cholestasis…

…Program for Amyotrophic Lateral Sclerosis (ALS) Genetic Testing Program for Familial Chylomicronemia Syndrome (FCS) Decode DEB Sponsored Testing Program Movement Disorder Genetic Test Program No-Cost Genetic Testing Program for Cholestasis…

…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 Pharmaceuticals, this program provides…

…with CNV PGxome $990 Familial Atrial Fibrillation Syndrome Panel Test Code Method Price 10323 Sequencing with CNV PGxome $990 Familial Chylomicronemia Panel Test Code Method Price 13025 Sequencing with CNV PGxome $990 Familial Cold…

…Syndrome Panel Test Code Method Price 10323 Sequencing 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…

…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…