Gastroenterology
| عنوان تست | کد تست | جزییات |
|---|---|---|
| Acute Intermittent Porphyria | 3161 | مشاهده |
| Acute Porphyria (Intermittent, Coproporphyria, Variegate ( | 3162 | مشاهده |
| Alpha.1 Antitrypsin | P3142 | مشاهده |
| Carnitine Palmitoyltransferase II Deficiency. via the CPT2 Gene | G31413 | مشاهده |
| Celiac disease | 3168 | مشاهده |
| Crigler-Najjar Syndrome | 31613 | مشاهده |
| Crohn disease | 31614 | مشاهده |
| Cystic. Fibrosis | G31421 | مشاهده |
| Familial Adenomatous. Polyposis | G31117 | مشاهده |
| Familial Intrahepatic Cholestasis | 31621 | مشاهده |
| Familial Mediterranean fever | G31622 | مشاهده |
| Fructose intolerance | 31623 | مشاهده |
| Gilbert Syndrome | 31625 | مشاهده |
| Hereditary Non.polyposis Colorectal Cancer | G31128 | مشاهده |
| Hereditary Pancreatitis | 31630 | مشاهده |
| Ankylosing spondylitis | 3165 | مشاهده |
| Lactose intolerance | 31634 | مشاهده |
| Wilson Disease | 31645 | مشاهده |
| Alagille Syndrome Panel | G3163 | مشاهده |
| Progressive Familial Intrahepatic Cholestasis (PFIC) and Alagille syndrome Panel | 31639 | مشاهده |
| Autoimmune Lymphoproliferative Syndrome.ALPS Panel | 3166 | مشاهده |
| Cholestasis Panel | 3169 | مشاهده |
| Congenital Anomalies of the Gastrointestinal Tract Panel | 31611 | مشاهده |
| Congenital Diarrhea and Enteropathies Panel | 31612 | مشاهده |
| Cystinuria Panel | G31616 | مشاهده |
| Glutaric Acidemia . Type II | G31430 | مشاهده |
| Medium Chain Acyl.CoA Dehydrogenase Deficiency via ACADM Gene | G31455 | مشاهده |
| Mitochondrial Trifunctional Protein Deficiency and Long-Chain 3.Hydroxyacyl CoA Dehydrogenase Deficiency Panel | G31462 | مشاهده |
| Short Chain Acyl.CoA Dehydrogenase Deficiency via the ACADS Gene | G31473 | مشاهده |
| Smith .Lemli-Opitz Syndrome via the DHCR7 Gene | G31474 | مشاهده |
| Systemic Primary Carnitine Deficiency .via the SLC22A5 Gene | G31475 | مشاهده |
| Very Long Chain Acyl.CoA Dehydrogenase Deficiency via the ACADVL Gene | G31644 | مشاهده |
| Glycogen Storage Disease (GSD) and Disorders. of Glucose Metabolism Panel | G31435 | مشاهده |
| Hirschsprung Disease (Non-syndromic) Panel | 31631 | مشاهده |
| Infantile Liver Failure Syndrome Panel | 31632 | مشاهده |
| Neuroblastoma .Panel | G31148 | مشاهده |
| Chronic Pancreatitis Panel | 31610 | مشاهده |
| Isolated Polycystic Liver Disease (PCLD) Panel | 31633 | مشاهده |
| Polycystic Liver Disease (PLD) Panel | 31638 | مشاهده |
| Rotor Syndrome Panel | 31640 | مشاهده |
| Epi. Met | G31115 | مشاهده |
| Disorders. of Fatty Acid Oxidation (FAOD) | G31424 | مشاهده |
| KRAS G12C.mutations | G31120 | مشاهده |
| Familial-Hemochromatosis | G31512 | مشاهده |
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