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: C0856825
Disease: Acute GVH disease
Acute GVH disease
disease Immune System Diseases Disease or Syndrome 294 49 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: 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: C0398620
Disease: Alpha-2-antiplasmin deficiency
Alpha-2-antiplasmin deficiency
disease Disease or Syndrome 2 0.010 None 1.000 1 1982 1982
ALPHA-2-PLASMIN INHIBITOR DEFICIENCY
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.920 strong 1.000 2 1989 2008
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3131 968 0.020 None 1.000 2 1991 2007
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: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
disease Cardiovascular Diseases Disease or Syndrome 566 78 0.030 None 1.000 3 3 2014 2019
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
disease Cardiovascular Diseases Disease or Syndrome 1995 266 0.010 None 1.000 1 2018 2018
CUI: C0004096
Disease: Asthma
Asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 1731 714 0.040 None 1.000 4 2015 2019
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
disease Cardiovascular Diseases Disease or Syndrome 1998 271 0.010 None 1.000 1 2018 2018
Attention deficit hyperactivity disorder
disease Mental Disorders Mental or Behavioral Dysfunction 532 215 0.010 None 1.000 1 2019 2019
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: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 233 27 0.070 None 1.000 7 1982 2008
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 211 5 0.010 None 1.000 1 2018 2018
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis
disease Infections; Respiratory Tract Diseases Disease or Syndrome 104 32 0.010 None 1.000 1 2017 2017
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 2827 321 0.010 None 1.000 1 2004 2004
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
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: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 676 123 0.010 None 1.000 1 1 2019 2019
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1515 412 0.010 None 1.000 1 2018 2018
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
disease Stomatognathic Diseases Disease or Syndrome 277 99 0.010 None 1.000 1 2019 2019
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 319 40 0.010 None 1.000 1 2018 2018
CUI: C1456399
Disease: Crushing sensation
Crushing sensation
phenotype Sign or Symptom 10 0.010 None 1.000 1 2017 2017
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 830 162 0.010 None 1.000 1 2010 2010