Cardiology
| عنوان تست | کد تست | جزییات |
|---|---|---|
| Alstrom. Syndrome | C3143 | مشاهده |
| CADASIL | 3177 | مشاهده |
| Cardiofaciocutaneous Syndrome | 3178 | مشاهده |
| Costello Syndrome | 3155 | مشاهده |
| Dilated Cardiomyopathy | 31713 | مشاهده |
| Fabry disease | 31718 | مشاهده |
| Fragile X Syndrome | C31514 | مشاهده |
| Gaucher disease | 31721 | مشاهده |
| LEOPARD Syndrome | 31733 | مشاهده |
| Long QT Syndrome | 31735 | مشاهده |
| Marfan. syndrome | C31526 | مشاهده |
| Noncompaction of Left Ventricular Myocardium | 31742 | مشاهده |
| Right Ventricular Arrhythmogenic Dysplasia | 31746 | مشاهده |
| Spinal. Muscular Atrophy | C31750 | مشاهده |
| Thrombophilia-markers | C31533 | مشاهده |
| Amyloidogenic Transthyretin Amyloidosis | 3173 | مشاهده |
| Brugada Syndrome | 3176 | مشاهده |
| Comprehensive Cardiac Arrhythmia | 31710 | مشاهده |
| Familial Atrial Fibrillation Syndrome | 31719 | مشاهده |
| Short QT Syndrome | 31748 | مشاهده |
| Sudden Cardiac Arrest | 31752 | مشاهده |
| Catecholaminergic Polymorphic Ventricular Tachycardia | 3179 | مشاهده |
| Comprehensive Cardiology | 31711 | مشاهده |
| Pan Cardiomyopathy | 31743 | مشاهده |
| Alagille .Syndrome | C3163 | مشاهده |
| Non-syndromic Congenital Heart Disease | C31464 | مشاهده |
| Noonan Spectrum Disorders-RASopathies | C31742 | مشاهده |
| Progressive Familial Intrahepatic Cholestasis (PFIC) and Alagille syndrome | C31639 | مشاهده |
| Disorders of Fatty .Acid Oxidation (FAOD) | C31424 | مشاهده |
| Medium Chain Acyl-CoA Dehydrogenase Deficiency | C31455 | مشاهده |
| Mitochondrial Trifunctional Protein Deficiency and Long-Chain 3.Hydroxyacyl CoA Dehydrogenase Deficiency | C31462 | مشاهده |
| Short Chain Acyl.CoA Dehydrogenase Deficiency via the ACADS | C31473 | مشاهده |
| Smith.Lemli.Opitz Syndrome via the DHCR7 Gene | C31474 | مشاهده |
| Systemic Primary Carnitine Deficiency | C31475 | مشاهده |
| Very Long Chain Acyl-CoA Dehydrogenase Deficiency via the Gene ACADVL | C31644 | مشاهده |
| Ectodermal Dysplasia | C31517 | مشاهده |
| Ellis-van Creveld Syndrome (EVC) | 31717 | مشاهده |
| Ehlers-Danlos Syndromes (EDS) | 31716 | مشاهده |
| Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum | 31722 | مشاهده |
| Hereditary Hemorrhagic Telangiectasia (HHT).Osler-Weber-Rendu Disease, and Capillary Malformation-Arteriovenous Malformation Syndrome (CM)-AVM | 31726 | مشاهده |
| Heterotaxy Situs Inversus and Kartagener's Syndrome | C31519 | مشاهده |
| X-linked Heterotaxy (HTX1) via the Gene ZIC3 | 31756 | مشاهده |
| Left Ventricular Noncompaction (LVNC) | 31732 | مشاهده |
| Loeys .Dietz Syndrome | C31734 | مشاهده |
| Marfan syndrome & Related Aortopathies (Exome) | C31737 | مشاهده |
| Pulmonary Arterial Hypertension (PAH) | C31745 | مشاهده |
| Stroke, Cerebral Hemorrhage, Hemiplegia, & Migraine | C31751 | مشاهده |
| Becker and Duchenne Muscular Dystrophies | C3147 | مشاهده |
| Comprehensive. Congenital Heart Disease | C31417 | مشاهده |
| Glutaric .Acidemia Type II via the ETFA Gene | C31432 | مشاهده |
| Glutaric Acidemia Type II via the .ETFB Gene | C31433 | مشاهده |
| Glutaric .Acidemia Type II via the ETFDH Gene | C31431 | مشاهده |
| Familial _Hemochromatosis | C31512 | مشاهده |
| Holt-Oram Syndrome | C31520 | مشاهده |
ساخته شده در آزمایشگاه جهش لب