F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
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: C0235430
Disease: Ketonemia
Ketonemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 4 0.010 None 1.000 1 1999 1999
CUI: C0584983
Disease: Homozygous Factor V Leiden mutation
Homozygous Factor V Leiden mutation 		disease Disease or Syndrome 1 0.010 None 1.000 1 1999 1999
CUI: C2314994
Disease: Infarction of spinal cord
Infarction of spinal cord 		disease Nervous System Diseases; Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome 14 1 0.010 None < 0.001 1 1999 1999
CUI: C0919631
Disease: Upper Extremity Deep Vein Thrombosis, Primary
Upper Extremity Deep Vein Thrombosis, Primary 		disease Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 1999 1999
CUI: C0024776
Disease: Maple Syrup Urine Disease
Maple Syrup Urine Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 24 134 0.010 None 1.000 1 1999 1999
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		disease Digestive System Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 1999 1999
CUI: C3845502
Disease: Myocardial infarction, stroke
Myocardial infarction, stroke 		disease Disease or Syndrome 46 3 0.010 None < 0.001 1 1999 1999
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 2346 222 0.010 None 1.000 1 1999 1999
CUI: C0042075
Disease: Urologic Diseases
Urologic Diseases 		group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 13 1 0.010 None 1.000 1 1999 1999
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 2084 288 0.010 None 1.000 1 1999 1999
CUI: C2363915
Disease: Cerebellar ischaemia
Cerebellar ischaemia 		disease Disease or Syndrome 4 0.010 None 1.000 1 1999 1999
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases 		group Cardiovascular Diseases Disease or Syndrome 35 4 0.020 None 1.000 2 2 1999 2000
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		group Cardiovascular Diseases Disease or Syndrome 688 40 0.020 None 1.000 2 1998 2000
CUI: C0040021
Disease: Thromboangiitis Obliterans
Thromboangiitis Obliterans 		disease Cardiovascular Diseases Disease or Syndrome 127 16 0.020 None 1.000 2 2 2000 2000
CUI: C1306889
Disease: Peripheral arterial occlusive disease
Peripheral arterial occlusive disease 		disease Cardiovascular Diseases Disease or Syndrome 35 3 0.010 None < 0.001 1 1 2000 2000
CUI: C0032807
Disease: Postphlebitic Syndrome
Postphlebitic Syndrome 		disease Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2000 2000
CUI: C2363755
Disease: Acquired Protein S Deficiency
Acquired Protein S Deficiency 		disease Hemic and Lymphatic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2000 2000
CUI: C0751202
Disease: Cystathionine beta-Synthase Deficiency Disease
Cystathionine beta-Synthase Deficiency Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases Disease or Syndrome 27 118 0.010 None 1.000 1 2001 2001
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 33 0.010 None 1.000 1 2001 2001
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 17 7 0.010 None 1.000 1 2001 2001
CUI: C0022346
Disease: Icterus
Icterus 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 241 17 0.010 None 1.000 1 2001 2001
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		disease Digestive System Diseases Disease or Syndrome 429 52 0.010 None 1.000 1 2001 2001
CUI: C1867596
Disease: Hyperprothrombinemia
Hyperprothrombinemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 4 0.020 None 1.000 2 2000 2002
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 13 6 0.010 None 1.000 1 2002 2002
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 988 363 0.010 None 1.000 1 2 2002 2002