SERPINC1, serpin family C member 1, 462

N. diseases: 184; N. variants: 46
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C4280702
Disease: Reduced antithrombin antigen
Reduced antithrombin antigen 		phenotype Finding 1 0.100 None 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		disease Cardiovascular Diseases Disease or Syndrome 5 0.100 None 0
CUI: C3279439
Disease: Recurrent spontaneous abortion
Recurrent spontaneous abortion 		phenotype Female Urogenital Diseases and Pregnancy Complications Finding 7 0.100 None 0
CUI: C3550150
Disease: Recurrent thrombophlebitis
Recurrent thrombophlebitis 		phenotype Cardiovascular Diseases Finding 5 0.100 None 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Pathologic Function 93 16 0.100 None 0
CUI: C4025286
Disease: Recurrent thromboembolism
Recurrent thromboembolism 		phenotype Cardiovascular Diseases Finding 2 0.100 None 0
CUI: C0264995
Disease: Occlusion of artery (disorder)
Occlusion of artery (disorder) 		phenotype Pathologic Function 3 0.100 None 0
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 76 15 0.100 None 0
CUI: C4552670
Disease: Portal Vein Thrombosis, CTCAE
Portal Vein Thrombosis, CTCAE 		phenotype Finding 7 0.100 None 0
CUI: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis 		phenotype Digestive System Diseases; Cardiovascular Diseases Pathologic Function 3 0.100 None 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		phenotype Finding 3 0.100 None 0
CUI: C0151942
Disease: Arterial thrombosis
Arterial thrombosis 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 33 1 0.100 None 0
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		group Hemic and Lymphatic Diseases Disease or Syndrome 267 31 0.300 None 1.000 1 1976 1976
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 11 0.110 None 1.000 1 1980 1980
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 14 9 0.010 None 1.000 1 1980 1980
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 15 7 0.310 None 1.000 2 1980 1983
CUI: C0936263
Disease: Cerebral Thrombus
Cerebral Thrombus 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.300 None 1.000 1 1983 1983
CUI: C0936261
Disease: Brain Thrombus
Brain Thrombus 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 1983 1983
CUI: C0752144
Disease: Brain Thrombosis
Brain Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.300 None 1.000 1 1983 1983
CUI: C0752143
Disease: Intracranial Thrombosis
Intracranial Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.300 None 1.000 1 1983 1983
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 122 78 0.300 None 1.000 1 1983 1983
CUI: C0272363
Disease: ANTICOAGULANT DISORDERS
ANTICOAGULANT DISORDERS 		group Hemic and Lymphatic Diseases Disease or Syndrome 1 0.010 None 1.000 1 1987 1987
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 208 136 0.010 None 1.000 1 1987 1987
CUI: C0553580
Disease: Ewings sarcoma
Ewings sarcoma 		disease Neoplasms Neoplastic Process 517 25 0.010 None 1.000 1 1987 1987
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.050 None 1.000 5 1981 1988