SERPINF2, serpin family F member 2, 5345

N. diseases: 104; N. variants: 7
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: C2752081
Disease: ALPHA-2-PLASMIN INHIBITOR DEFICIENCY
ALPHA-2-PLASMIN INHIBITOR DEFICIENCY 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 2 0.920 strong 1.000 7 2 1989 2008
CUI: C0477316
Disease: Other specified coagulation defects
Other specified coagulation defects 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.200 None 1.000 2 1999 1999
CUI: C0233524
Disease: Falsification
Falsification 		disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2019 2019
CUI: C0019123
Disease: Hemothorax
Hemothorax 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Pathologic Function 1 0.100 None 0
CUI: C3489734
Disease: Anti-plasmin deficiency, congenital
Anti-plasmin deficiency, congenital 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 0
CUI: C4280701
Disease: Reduced euglobulin clot lysis time
Reduced euglobulin clot lysis time 		phenotype Finding 1 0.100 None 0
CUI: C0272274
Disease: Familial hemorrhagic diathesis
Familial hemorrhagic diathesis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1982 1982
CUI: C0333274
Disease: Purulent discharge
Purulent discharge 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2009 2009
CUI: C0398620
Disease: Alpha-2-antiplasmin deficiency
Alpha-2-antiplasmin deficiency 		disease Disease or Syndrome 2 0.010 None 1.000 1 1982 1982
CUI: C0333208
Disease: Fibrin thrombus
Fibrin thrombus 		disease Cardiovascular Diseases Acquired Abnormality 4 0.010 None 1.000 1 2018 2018
CUI: C4023145
Disease: Abnormal umbilical stump bleeding
Abnormal umbilical stump bleeding 		disease Anatomical Abnormality 5 0.100 None 0
CUI: C0240412
Disease: Muscle hematoma
Muscle hematoma 		disease Pathological Conditions, Signs and Symptoms Injury or Poisoning 6 0.100 None 0
CUI: C0085082
Disease: Fungemia
Fungemia 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 7 0.010 None 1.000 1 2007 2007
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 3 0.010 None 1.000 1 2017 2017
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma 		phenotype Finding 9 0.100 None 0
CUI: C1456399
Disease: Crushing sensation
Crushing sensation 		phenotype Sign or Symptom 10 0.010 None 1.000 1 2017 2017
CUI: C3826157
Disease: Hypertension in children
Hypertension in children 		disease Disease or Syndrome 12 0.020 None 1.000 2 2017 2019
CUI: C1112433
Disease: Thromboembolic stroke
Thromboembolic stroke 		disease Cardiovascular Diseases Disease or Syndrome 13 1 0.010 None 1.000 1 2018 2018
CUI: C0018924
Disease: Hemarthrosis
Hemarthrosis 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Pathologic Function 13 0.100 None 0
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 16 46 0.010 None 1.000 1 1993 1993
CUI: C2931672
Disease: Cerebral hemorrhage with amyloidosis, hereditary, Dutch type
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 20 2 0.010 None 1.000 1 1992 1992
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		group Hemic and Lymphatic Diseases Disease or Syndrome 30 3 0.040 None 1.000 4 1982 2002
CUI: C0038395
Disease: Streptococcal Infections
Streptococcal Infections 		group Infections Disease or Syndrome 34 0.100 None 0.957 23 1998 2019
CUI: C0038160
Disease: Staphylococcal Infections
Staphylococcal Infections 		group Infections Disease or Syndrome 37 5 0.100 None 0.895 19 1988 2017
CUI: C0151699
Disease: Intracranial Hemorrhage
Intracranial Hemorrhage 		group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 40 2 0.100 None 0