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: C0242339
Disease: Dyslipidemias
Dyslipidemias 		group Nutritional and Metabolic Diseases Disease or Syndrome 471 184 0.010 None 1.000 1 2018 2018
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: 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: C2363915
Disease: Cerebellar ischaemia
Cerebellar ischaemia 		disease Disease or Syndrome 4 0.010 None 1.000 1 1999 1999
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		disease Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2003 2003
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 2689 322 0.010 None 1.000 1 2018 2018
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 36 0.010 None 1.000 1 2002 2002
CUI: C0235522
Disease: Disorder of vein
Disorder of vein 		group Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 16 1 0.010 None < 0.001 1 2010 2010
CUI: C0235430
Disease: Ketonemia
Ketonemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 4 0.010 None 1.000 1 1999 1999
CUI: C0232726
Disease: Rectal tenesmus
Rectal tenesmus 		phenotype Digestive System Diseases; Nervous System Diseases Sign or Symptom 3 0.010 None 1.000 1 2018 2018
CUI: C0221505
Disease: Lesion of brain
Lesion of brain 		group Disease or Syndrome 188 9 0.010 None 1.000 1 1 2006 2006
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		disease Neoplasms; Stomatognathic Diseases Neoplastic Process 734 172 0.010 None 1.000 1 2005 2005
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 15 7 0.010 None 1.000 1 2 2010 2010
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 62 78 0.010 None 1.000 1 2 2010 2010
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: C0034155
Disease: Purpura, Thrombotic Thrombocytopenic
Purpura, Thrombotic Thrombocytopenic 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 80 13 0.010 None 1.000 1 2020 2020
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 198 59 0.010 None 1.000 1 2 2006 2006
CUI: C0034069
Disease: Pulmonary Fibrosis
Pulmonary Fibrosis 		disease Respiratory Tract Diseases Disease or Syndrome 924 25 0.010 None 1.000 1 2002 2002
CUI: C0033626
Disease: Protein Deficiency
Protein Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 125 2 0.010 None 1.000 1 2004 2004
CUI: C0032962
Disease: Pregnancy Complications
Pregnancy Complications 		group Female Urogenital Diseases and Pregnancy Complications Pathologic Function 13 0.010 None 1.000 1 2006 2006
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia 		phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 166 14 0.010 None 1.000 1 2005 2005
CUI: C0032807
Disease: Postphlebitic Syndrome
Postphlebitic Syndrome 		disease Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2000 2000
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 254 51 0.010 None 1.000 1 2019 2019
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
CUI: C0032320
Disease: Pneumoperitoneum
Pneumoperitoneum 		disease Digestive System Diseases Disease or Syndrome 28 0.010 None 1.000 1 2019 2019