更多...
收起
FGA基因(以及对应的蛋白质)的细胞分布位置:
FGA基因的本体(GO)信息:
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
Amyloidosis, familial visceral | 0.36 | 1 | 4 | CLINVAR_CTD_human_UNIPROT |
Dysfibrinogenemia, Congenital | 0.24 | 2 | 0 | ORPHANET_UNIPROT |
Congenital hypofibrinogenemia | 0.24 | 1 | 0 | ORPHANET_UNIPROT |
Pulmonary Embolism | 0.2 | 2 | 0 | CTD_human_RGD |
Fibrinogen Adverse Event | 0.134202192 | 5 | 3 | GAD_GWASCAT |
Venous Thromboembolism | 0.132192478 | 4 | 0 | CTD_human_GAD_LHGDN |
Thrombosis | 0.129468128 | 5 | 0 | CTD_human_GAD |
Afibrinogenemia | 0.123810118 | 8 | 0 | BeFree_CTD_human_LHGDN |
Dysfibrinogenemia | 0.120542884 | 2 | 2 | BeFree_CLINVAR |
Cholestasis | 0.12 | 1 | 0 | CTD_human |
Kidney Diseases | 0.12 | 2 | 0 | CTD_human |
Mouth Neoplasms | 0.12 | 1 | 0 | CTD_human |
Osteoporosis | 0.12 | 1 | 0 | CTD_human |
Adverse reaction to drug | 0.12 | 1 | 0 | CTD_human |
Thrombophilia | 0.12 | 1 | 0 | CTD_human |
Amyloidosis, Familial | 0.12 | 2 | 0 | CTD_human |
Drug-Induced Liver Injury | 0.12 | 1 | 0 | CTD_human |
Hypodysfibrinogenemia, Congenital | 0.12 | 0 | 1 | CLINVAR |
Diabetes Mellitus, Experimental | 0.08 | 1 | 0 | RGD |
Pancreatitis | 0.08 | 1 | 0 | RGD |
Sepsis | 0.08 | 1 | 0 | RGD |
Acute kidney injury | 0.08 | 1 | 0 | RGD |
Myocardial Infarction | 0.024656398 | 8 | 0 | BeFree_GAD_LHGDN |
Cerebrovascular accident | 0.020193776 | 7 | 0 | BeFree_GAD_LHGDN |
Brain Ischemia | 0.01183516 | 5 | 0 | GAD |
Hypertensive disease | 0.00973957 | 4 | 0 | BeFree_GAD |
Cardiovascular Diseases | 0.008001298 | 3 | 0 | BeFree_GAD_LHGDN |
Venous Thrombosis | 0.007101096 | 3 | 1 | GAD |
Amyloidosis | 0.005720142 | 3 | 0 | BeFree_LHGDN |
Ischemic stroke | 0.005276948 | 4 | 0 | BeFree_GAD |
Cerebrovascular Disorders | 0.005091382 | 2 | 0 | GAD_LHGDN |
Vascular Diseases | 0.005091382 | 2 | 0 | GAD_LHGDN |
Atherosclerosis | 0.005005506 | 3 | 0 | BeFree_GAD |
Deep Vein Thrombosis | 0.005005506 | 3 | 1 | BeFree_GAD |
Amyloid nephropathy | 0.002909916 | 2 | 0 | BeFree_GAD |
Factor V Deficiency | 0.00272435 | 1 | 0 | LHGDN |
Pulmonary Hypertension | 0.00272435 | 1 | 0 | LHGDN |
Lung Neoplasms | 0.00272435 | 1 | 0 | LHGDN |
Hereditary factor I deficiency disease | 0.002714419 | 10 | 0 | BeFree |
Cerebral Infarction | 0.002638474 | 2 | 0 | BeFree_GAD |
Thromboembolism | 0.002638474 | 2 | 0 | BeFree_GAD |
Alzheimer's Disease | 0.002367032 | 1 | 0 | GAD |
Anemia, Sickle Cell | 0.002367032 | 1 | 0 | GAD |
Angina Pectoris | 0.002367032 | 1 | 0 | GAD |
Carotid Artery Diseases | 0.002367032 | 1 | 0 | GAD |
Carotid Stenosis | 0.002367032 | 1 | 0 | GAD |
Diabetes Mellitus, Non-Insulin-Dependent | 0.002367032 | 1 | 0 | GAD |
Foramen Ovale, Patent | 0.002367032 | 1 | 0 | GAD |
Hemorrhage | 0.002367032 | 1 | 0 | GAD |
Ischemia | 0.002367032 | 1 | 0 | GAD |
Obesity | 0.002367032 | 1 | 0 | GAD |
Age related macular degeneration | 0.002367032 | 1 | 0 | GAD |
Acute Coronary Syndrome | 0.002367032 | 1 | 0 | GAD |
Coronary Artery Disease | 0.002367032 | 1 | 0 | GAD |
Cerebral Hemorrhage | 0.002367032 | 1 | 0 | GAD |
Ischemic Cerebrovascular Accident | 0.000542884 | 2 | 0 | BeFree |
Arteriosclerosis | 0.000271442 | 1 | 0 | BeFree |
Endometriosis | 0.000271442 | 1 | 0 | BeFree |
Muscle Rigidity | 0.000271442 | 1 | 0 | BeFree |
Nephrotic Syndrome | 0.000271442 | 1 | 0 | BeFree |
Neuroblastoma | 0.000271442 | 1 | 0 | BeFree |
Arterial thrombosis | 0.000271442 | 1 | 0 | BeFree |
Deep thrombophlebitis | 0.000271442 | 1 | 1 | BeFree |
Amyloidosis, Hereditary | 0.000271442 | 1 | 0 | BeFree |
Hypodysfibrinogenemia | 0.000271442 | 1 | 0 | BeFree |
Hypofibrinogenemia | 0.000271442 | 1 | 0 | BeFree |
Central neuroblastoma | 0.000271442 | 1 | 0 | BeFree |
忘记密码? 点击找回密码.
扫一扫右方二维码,关注微信订阅号,实时查看信息,关注医学生物学动态。