F7, coagulation factor VII, 2155

N. diseases: 99; N. variants: 88
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: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 10 73 0.740 definitive 1.000 53 71 1988 2019
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 117 218 0.500 None 1.000 2 2003 2006
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1800 680 0.400 None 1.000 12 3 1995 2006
CUI: C0151699
Disease: Intracranial Hemorrhage
Intracranial Hemorrhage
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 40 2 0.400 None 1.000 5 2004 2010
CUI: C0019080
Disease: Hemorrhage
Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 47 0.310 None 1.000 4 2003 2007
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 122 78 0.310 None 1.000 3 2006 2011
CUI: C0751893
Disease: Posterior Fossa Hemorrhage
Posterior Fossa Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 5 0.300 None 1.000 5 2004 2010
CUI: C0553692
Disease: Brain hemorrhage
Brain hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 10 0.300 None 1.000 5 2004 2010
CUI: C0749098
Disease: Hematoma, Subdural, Acute
Hematoma, Subdural, Acute
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases; Wounds and Injuries Pathologic Function 1 0.300 None 1.000 1 2002 2002
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
phenotype Cardiovascular Diseases Pathologic Function 25 3 0.300 None 1.000 1 2010 2010
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
disease Cardiovascular Diseases Disease or Syndrome 230 93 0.300 None 1.000 1 2003 2003
CUI: C0032787
Disease: Postoperative Complications
Postoperative Complications
group Pathological Conditions, Signs and Symptoms Pathologic Function 5 0.300 None 1.000 1 2003 2003
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 30 3 0.300 None 1.000 1 2006 2006
CUI: C0018965
Disease: Hematuria
Hematuria
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 235 31 0.300 None 1.000 1 2006 2006
CUI: C0751797
Disease: Intracranial Hematoma, Traumatic
Intracranial Hematoma, Traumatic
phenotype Nervous System Diseases; Cardiovascular Diseases; Wounds and Injuries Pathologic Function 1 0.300 None 1.000 1 2010 2010
Disseminated Intravascular Coagulation
disease Hemic and Lymphatic Diseases Disease or Syndrome 117 3 0.300 None 1.000 1 2005 2005
MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
phenotype Finding 9 3 0.300 None 0
CUI: C0243026
Disease: Sepsis
Sepsis
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1453 144 0.210 None 1.000 3 1987 2002
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.210 None 1.000 2 2 1976 2004
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Experimental Model of Disease 522 0.200 None 1.000 2 2001 2006
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
group Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 2803 824 0.200 None 1.000 2 1 2000 2000
CUI: C0020476
Disease: Hyperlipoproteinemias
Hyperlipoproteinemias
disease Nutritional and Metabolic Diseases Disease or Syndrome 49 7 0.200 None 1.000 1 2001 2001
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 13 0.200 None 1.000 1 1989 1989
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 613 283 0.200 None 1.000 1 1976 1976
Diabetes Mellitus, Non-Insulin-Dependent
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 3134 2672 0.200 None 1.000 1 2 2003 2003