F12, coagulation factor XII, 2161

N. diseases: 87; N. variants: 22
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: C0015526
Disease: Factor XII Deficiency
Factor XII Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 14 13 0.970 definitive 1.000 28 12 1979 2019
CUI: C1857728
Disease: Hereditary Angioedema Type III
Hereditary Angioedema Type III
disease Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 4 3 0.740 moderate 1.000 14 3 1987 2019
CUI: C0019243
Disease: Angioedemas, Hereditary
Angioedemas, Hereditary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 54 7 0.700 strong 0.952 21 2 1984 2019
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.400 None 1.000 1 1 1984 1984
CUI: C0019208
Disease: Hepatoma, Novikoff
Hepatoma, Novikoff
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 125 0.300 None 1.000 1 2001 2001
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
phenotype Cardiovascular Diseases Pathologic Function 25 3 0.300 None 1.000 1 2005 2005
CUI: C0086404
Disease: Experimental Hepatoma
Experimental Hepatoma
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 117 0.300 None 1.000 1 2001 2001
CUI: C0023904
Disease: Liver Neoplasms, Experimental
Liver Neoplasms, Experimental
phenotype Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 152 0.300 None 1.000 1 2001 2001
CUI: C0019207
Disease: Hepatoma, Morris
Hepatoma, Morris
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 124 0.300 None 1.000 1 2001 2001
Hereditary angioedema with normal C1 esterase inhibitor activity
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.300 None 1.000 1 2010 2010
CUI: C0376618
Disease: Endotoxemia
Endotoxemia
phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 401 5 0.200 None 1.000 1 2000 2000
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 246 45 0.200 None 1.000 1 2005 2005
Activated Partial Thromboplastin Time measurement
phenotype Laboratory Procedure 17 44 0.100 None 1.000 2 3 2013 2018
CUI: C1629609
Disease: Age at menopause
Age at menopause
phenotype Finding 129 209 0.100 None 1.000 1 1 2019 2019
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
phenotype Laboratory Procedure 433 3282 0.100 None 1.000 1 1 2012 2012
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 2 2018 2018
CUI: C2697764
Disease: Interleukin 16 Measurement
Interleukin 16 Measurement
phenotype Laboratory Procedure 9 12 0.100 None 1.000 1 1 2017 2017
CUI: C0883409
Disease: Cardiac troponin I measurement
Cardiac troponin I measurement
phenotype Laboratory Procedure 11 14 0.100 None 1.000 1 1 2019 2019
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
phenotype Laboratory Procedure 55 427 0.100 None 1.000 1 1 2013 2013
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
disease Neoplasms Neoplastic Process 3111 6892 0.100 None 1.000 1 1 2017 2017
Partial thromboplastin time increased (finding)
phenotype Finding 18 1 0.100 None 0
CUI: C0042109
Disease: Urticaria
Urticaria
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 168 11 0.100 None 0 1
CUI: C0151563
Disease: Prolonged whole-blood clotting time
Prolonged whole-blood clotting time
phenotype Hemic and Lymphatic Diseases Finding 4 0.100 None 0
CUI: C0236024
Disease: Edema of pharynx
Edema of pharynx
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases Pathologic Function 2 0.100 None 0
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding)
phenotype Pathological Conditions, Signs and Symptoms Finding 14 8 0.100 None 0 1