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: C0750384
Disease: Coumarin Resistance
Coumarin Resistance
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 10 0.800 strong 0.933 15 8 2004 2018
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 1 1 0.700 strong 1.000 3 1 2004 2011
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.370 None 0.857 7 2 2006 2019
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
disease Cardiovascular Diseases Disease or Syndrome 1576 1178 0.340 None 1.000 4 1 2006 2013
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases
group Cardiovascular Diseases Disease or Syndrome 688 40 0.320 None 1.000 2 2006 2007
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 4 0.310 None 1.000 2 2004 2016
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 2006 2014
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 267 31 0.310 None 1.000 2 1 2008 2008
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
WARFARIN SENSITIVITY (disorder)
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 8 0.300 None 1.000 17 2 2004 2019
CUI: C0019080
Disease: Hemorrhage
Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 47 0.300 None 1.000 2 2010 2015
CUI: C0741160
Disease: Aortic Aneurysm, Ruptured
Aortic Aneurysm, Ruptured
disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome 13 1 0.300 None 1.000 1 2006 2006
CUI: C0041755
Disease: Adverse reaction to drug
Adverse reaction to drug
group Chemically-Induced Disorders Pathologic Function 87 0.300 None 1.000 1 2015 2015
CUI: C0040053
Disease: Thrombosis
Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 98 0.300 None 1.000 1 2018 2018
CUI: C0013221
Disease: Drug toxicity
Drug toxicity
group Chemically-Induced Disorders Injury or Poisoning 86 0.300 None 1.000 1 2015 2015
CUI: C0003496
Disease: Aortic Rupture
Aortic Rupture
disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome 22 0.300 None 1.000 1 2006 2006
CUI: C0087086
Disease: Thrombus
Thrombus
phenotype Cardiovascular Diseases Pathologic Function 46 0.300 None 1.000 1 2018 2018
CUI: C1096249
Disease: Calcification of the aorta
Calcification of the aorta
phenotype Pathologic Function 21 0.200 None 1.000 1 2008 2008
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
phenotype Finding 90 119 0.100 None 1.000 1 1 2019 2019
CUI: C4280698
Disease: Reduced prothrombin antigen
Reduced prothrombin antigen
phenotype Finding 2 0.100 None 0
CUI: C4024722
Disease: Reduced factor VII activity
Reduced factor VII activity
phenotype Finding 4 0.100 None 0
CUI: C4024702
Disease: Reduced factor X activity
Reduced factor X activity
phenotype Finding 3 0.100 None 0
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency
phenotype Hemic and Lymphatic Diseases Pathologic Function 71 14 0.100 None 0
CUI: C4023159
Disease: Reduced factor IX activity
Reduced factor IX activity
phenotype Finding 5 0.100 None 0
Abnormality of metabolism/homeostasis
phenotype Finding 171 5 0.100 None 0
Abnormality of blood and blood-forming tissues
disease Finding 23 1 0.100 None 0