SERPINF2, serpin family F member 2, 5345

N. diseases: 79; N. variants: 3
Source: BEFREE ×
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 0.920 strong 1.000 2 1989 2008
CUI: C0233524
Disease: Falsification
Falsification 		disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2019 2019
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: 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: C1456399
Disease: Crushing sensation
Crushing sensation 		phenotype Sign or Symptom 10 0.010 None 1.000 1 2017 2017
CUI: C1112433
Disease: Thromboembolic stroke
Thromboembolic stroke 		disease Cardiovascular Diseases Disease or Syndrome 11 1 0.010 None 1.000 1 2018 2018
CUI: C3826157
Disease: Hypertension in children
Hypertension in children 		disease Disease or Syndrome 12 0.020 None 1.000 2 2017 2019
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 13 2 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 26 3 0.040 None 1.000 4 1982 2002
CUI: C0038160
Disease: Staphylococcal Infections
Staphylococcal Infections 		group Infections Disease or Syndrome 31 1 0.100 None 0.895 19 1988 2017
CUI: C0038395
Disease: Streptococcal Infections
Streptococcal Infections 		group Infections Disease or Syndrome 34 0.100 None 0.957 23 1998 2019
CUI: C0080233
Disease: Tooth Loss
Tooth Loss 		disease Stomatognathic Diseases Acquired Abnormality 49 8 0.020 None 1.000 2 2018 2019
CUI: C0019243
Disease: Angioedemas, Hereditary
Angioedemas, Hereditary 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 53 7 0.020 None 1.000 2 1984 1985
CUI: C4025886
Disease: Severe periodontitis
Severe periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 53 12 0.010 None 1.000 1 2018 2018
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 61 14 0.010 None 1.000 1 2017 2017
CUI: C4551689
Disease: Sleep-Disordered Breathing
Sleep-Disordered Breathing 		disease Respiratory Tract Diseases; Nervous System Diseases Disease or Syndrome 64 0.010 None 1.000 1 2019 2019
CUI: C0476227
Disease: pricking of skin
pricking of skin 		phenotype Sign or Symptom 65 1 0.010 None 1.000 1 2018 2018
CUI: C0034155
Disease: Purpura, Thrombotic Thrombocytopenic
Purpura, Thrombotic Thrombocytopenic 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 77 12 0.010 None 1.000 1 2014 2014
CUI: C1266184
Disease: Atypical Teratoid Rhabdoid Tumor
Atypical Teratoid Rhabdoid Tumor 		disease Neoplasms Neoplastic Process 83 0.010 None 1.000 1 2017 2017
CUI: C0035455
Disease: Rhinitis
Rhinitis 		disease Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 94 18 0.010 None 1.000 1 2018 2018