F5, coagulation factor V, 2153

N. diseases: 369; N. variants: 52
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: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 7 7 0.780 strong 1.000 20 7 1994 2019
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 6 0.730 definitive 1.000 29 6 1988 2018
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome
disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 24 4 0.700 None 1.000 14 1 1996 2018
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis
disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 23 4 0.600 None 1.000 12 1 1996 2018
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
phenotype Cardiovascular Diseases Disease or Syndrome 378 408 0.500 None 0.964 194 14 1995 2020
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
disease Cardiovascular Diseases Disease or Syndrome 230 93 0.500 None 1.000 74 5 1996 2018
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.500 None 0.971 35 2 1995 2016
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 117 218 0.500 None 1.000 22 11 2002 2012
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1800 680 0.400 None 0.962 26 2 1995 2019
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 267 31 0.400 None 0.933 15 1 1996 2014
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary
disease Hemic and Lymphatic Diseases Disease or Syndrome 17 9 0.400 None 1.000 11 2 1997 2018
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1
phenotype Finding 1 1 0.400 None 0 1
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion
disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 76 15 0.390 None 1.000 10 1 1998 2017
CUI: C0040053
Disease: Thrombosis
Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 98 0.380 None 1.000 10 1997 2007
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 687 123 0.340 None 1.000 4 1 1995 2009
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
phenotype Cardiovascular Diseases Pathologic Function 25 3 0.320 None 1.000 4 2003 2010
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1182 189 0.320 None 1.000 3 1 2003 2008
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 155 2 0.310 None 1.000 2 1995 2004
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 358 5 0.310 None 1.000 2 2004 2007
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.310 None 1.000 1 2011 2011
CUI: C0087086
Disease: Thrombus
Thrombus
phenotype Cardiovascular Diseases Pathologic Function 46 0.300 None 1.000 2 1997 2000
CUI: C2713443
Disease: Familial Intestinal Polyposis
Familial Intestinal Polyposis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 16 0.300 None 1.000 1 2014 2014
CUI: C2713442
Disease: Polyposis, Adenomatous Intestinal
Polyposis, Adenomatous Intestinal
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 16 332 0.300 None 1.000 1 2014 2014
CUI: C3852984
Disease: Acute Mesenteric Arterial Embolus
Acute Mesenteric Arterial Embolus
disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.300 None 1.000 1 2013 2013
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1179 64 0.300 None 1.000 1 2008 2008