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: 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: C0333519
Disease: Caries (morphologic abnormality)
Caries (morphologic abnormality) 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 106 33 0.010 None 1.000 1 2018 2018
CUI: C0333274
Disease: Purulent discharge
Purulent discharge 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2009 2009
CUI: C0333208
Disease: Fibrin thrombus
Fibrin thrombus 		disease Cardiovascular Diseases Acquired Abnormality 4 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: 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: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 277 99 0.010 None 1.000 1 2019 2019
CUI: C0237123
Disease: Alcohol or Other Drugs use
Alcohol or Other Drugs use 		disease Mental or Behavioral Dysfunction 108 21 0.010 None 1.000 1 2018 2018
CUI: C0233524
Disease: Falsification
Falsification 		disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2019 2019
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		group Respiratory Tract Diseases Disease or Syndrome 277 32 0.010 None 1.000 1 2017 2017
CUI: C0162678
Disease: Neurofibromatoses
Neurofibromatoses 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Neoplastic Process 134 5 0.010 None 1.000 1 1989 1989
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute 		disease Digestive System Diseases Disease or Syndrome 236 14 0.010 None 1.000 1 2018 2018
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 217 76 0.010 None 1.000 1 2019 2019
CUI: C0085281
Disease: Addictive Behavior
Addictive Behavior 		phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 330 54 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: C0042029
Disease: Urinary tract infection
Urinary tract infection 		group Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 215 14 0.010 None 1.000 1 2010 2010
CUI: C0343401
Disease: MRSA - Methicillin resistant Staphylococcus aureus infection
MRSA - Methicillin resistant Staphylococcus aureus infection 		disease Infections Disease or Syndrome 222 1 0.010 None 1.000 1 2007 2007
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: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 3 0.010 None 1.000 1 2017 2017
CUI: C4025886
Disease: Severe periodontitis
Severe periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 53 12 0.010 None 1.000 1 2018 2018
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: 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: C1456399
Disease: Crushing sensation
Crushing sensation 		phenotype Sign or Symptom 10 0.010 None 1.000 1 2017 2017
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 427 94 0.010 None 1.000 1 2019 2019
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 861 362 0.010 None 1.000 1 2019 2019