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: 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: 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: 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: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		phenotype Cardiovascular Diseases Disease or Syndrome 378 408 0.300 None 1.000 1 1991 1991
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: 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: C0344315
Disease: Depressed mood
Depressed mood 		phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1461 269 0.010 None 1.000 1 2019 2019
CUI: C0333875
Disease: High-Grade Squamous Intraepithelial Lesions
High-Grade Squamous Intraepithelial Lesions 		phenotype Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 150 8 0.010 None 1.000 1 2004 2004
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: C0162429
Disease: Malnutrition
Malnutrition 		disease Nutritional and Metabolic Diseases Disease or Syndrome 417 29 0.010 None 1.000 1 2009 2009
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases 		group Cardiovascular Diseases Disease or Syndrome 150 18 0.010 None 1.000 1 2009 2009
CUI: C0265101
Disease: Carotid artery occlusion
Carotid artery occlusion 		phenotype Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 74 1 0.010 None 1.000 1 2004 2004
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		disease Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 1553 320 0.010 None 1.000 1 2019 2019
CUI: C0375023
Disease: Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site 		disease Disease or Syndrome 467 14 0.010 None < 0.001 1 2018 2018
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: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 219 79 0.010 None 1.000 1 2009 2009
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: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 1224 129 0.010 None 1.000 1 2019 2019
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: C1512409
Disease: Hepatocarcinogenesis
Hepatocarcinogenesis 		disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 855 24 0.010 None 1.000 1 2009 2009
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		group Cardiovascular Diseases Disease or Syndrome 319 128 0.010 None 1.000 1 2009 2009
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