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: C3489734
Disease: Anti-plasmin deficiency, congenital
Anti-plasmin deficiency, congenital 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 0
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: C0020476
Disease: Hyperlipoproteinemias
Hyperlipoproteinemias 		disease Nutritional and Metabolic Diseases Disease or Syndrome 49 7 0.200 None 1.000 1 1990 1990
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 472 83 0.200 None 1.000 1 1990 1990
CUI: C0267941
Disease: Pancreatitis, Acute Necrotizing
Pancreatitis, Acute Necrotizing 		disease Digestive System Diseases Disease or Syndrome 62 1 0.200 None 1.000 1 1999 1999
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: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		disease Finding 578 1158 0.100 None 1.000 1 1 2018 2018
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		phenotype Laboratory Procedure 433 3282 0.100 None 1.000 1 1 2018 2018
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		disease Musculoskeletal Diseases Anatomical Abnormality 656 1178 0.100 None 1.000 1 1 2018 2018
CUI: C0022336
Disease: Creutzfeldt-Jakob disease
Creutzfeldt-Jakob disease 		disease Infections; Nervous System Diseases; Mental Disorders Disease or Syndrome 137 52 0.100 None 1.000 1 1 2012 2012
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		phenotype Laboratory Procedure 264 1463 0.100 None 1.000 1 1 2019 2019
CUI: C0240412
Disease: Muscle hematoma
Muscle hematoma 		disease Pathological Conditions, Signs and Symptoms Injury or Poisoning 6 0.100 None 0
CUI: C0019123
Disease: Hemothorax
Hemothorax 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Pathologic Function 1 0.100 None 0
CUI: C0151825
Disease: Bone pain
Bone pain 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Sign or Symptom 139 0.100 None 0
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
CUI: C0018965
Disease: Hematuria
Hematuria 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 235 31 0.100 None 0
CUI: C0018924
Disease: Hemarthrosis
Hemarthrosis 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Pathologic Function 13 0.100 None 0
CUI: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise 		phenotype Wounds and Injuries Finding 133 14 0.100 None 0
CUI: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Pathologic Function 50 2 0.100 None 0
CUI: C4554063
Disease: Bone Pain, CTCAE 5.0
Bone Pain, CTCAE 5.0 		phenotype Finding 67 0.100 None 0
CUI: C4280701
Disease: Reduced euglobulin clot lysis time
Reduced euglobulin clot lysis time 		phenotype Finding 1 0.100 None 0
CUI: C4023145
Disease: Abnormal umbilical stump bleeding
Abnormal umbilical stump bleeding 		disease Anatomical Abnormality 5 0.100 None 0
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma 		phenotype Finding 9 0.100 None 0