SERPIND1, serpin family D member 1, 3053

N. diseases: 60; N. variants: 5
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: C2676505
Disease: Post-angioplasty coronary artery restenosis
Post-angioplasty coronary artery restenosis 		phenotype Cardiovascular Diseases Finding 1 0.100 None 0
CUI: C1735901
Disease: Recurrent deep vein thrombosis
Recurrent deep vein thrombosis 		phenotype Cardiovascular Diseases Pathologic Function 2 0.100 None 0
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 161 43 0.320 None 1.000 3 1987 1999
CUI: C0023895
Disease: Liver diseases
Liver diseases 		group Digestive System Diseases Disease or Syndrome 1019 100 0.010 None 1.000 1 1987 1987
CUI: C0398626
Disease: Heparin cofactor II deficiency (disorder)
Heparin cofactor II deficiency (disorder) 		disease Cardiovascular Diseases Disease or Syndrome 4 5 0.700 strong 1.000 4 5 1989 2004
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 1991 1991
CUI: C0025472
Disease: Mesenteric Vascular Occlusion
Mesenteric Vascular Occlusion 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.300 None 1.000 1 1991 1991
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		phenotype Cardiovascular Diseases Disease or Syndrome 378 408 0.300 None 1.000 1 1991 1991
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 46 0.010 None 1.000 1 1996 1996
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 43 14 0.010 None 1.000 1 1996 1996
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 1998 1998
CUI: C4290046
Disease: trachomatis
trachomatis 		disease Disease or Syndrome 175 7 0.030 None 1.000 3 1999 2019
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 230 93 0.020 None 1.000 2 1999 2004
CUI: C0040028
Disease: Thrombocythemia, Essential
Thrombocythemia, Essential 		disease Hemic and Lymphatic Diseases Disease or Syndrome 220 37 0.010 None 1.000 1 1999 1999
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		disease Hemic and Lymphatic Diseases Disease or Syndrome 117 3 0.110 None 1.000 1 1999 1999
CUI: C0019880
Disease: Homocystinuria
Homocystinuria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases Disease or Syndrome 39 27 0.010 None 1.000 1 1999 1999
CUI: C0750989
Disease: External Carotid Artery Thrombosis
External Carotid Artery Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 2002 2002
CUI: C0750990
Disease: Internal Carotid Artery Thrombosis
Internal Carotid Artery Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 2002 2002
CUI: C0007274
Disease: Carotid Artery Thrombosis
Carotid Artery Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 30 0.300 None 1.000 1 2002 2002
CUI: C0750988
Disease: Common Carotid Artery Thrombosis
Common Carotid Artery Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 2002 2002
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection 		disease Infections Disease or Syndrome 429 42 0.060 None 1.000 6 2003 2017
CUI: C0333873
Disease: Squamous intraepithelial lesion
Squamous intraepithelial lesion 		phenotype Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 73 8 0.010 None 1.000 1 2003 2003
CUI: C1302773
Disease: Low Grade Squamous Intraepithelial Neoplasia
Low Grade Squamous Intraepithelial Neoplasia 		disease Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 94 2 0.030 None 1.000 3 2004 2008
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		disease Cardiovascular Diseases Disease or Syndrome 2006 267 0.030 None 1.000 3 2004 2016
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		disease Cardiovascular Diseases Disease or Syndrome 2044 281 0.030 None 1.000 3 2004 2016