VWF, von Willebrand factor, 7450

N. diseases: 498; N. variants: 158
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: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise
phenotype Wounds and Injuries Finding 133 14 0.100 None 0
VON WILLEBRAND FACTOR VICENZA PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery
phenotype Pathologic Function 11 0.100 None 0
Reduced quantity of Von Willebrand factor
phenotype Finding 2 1 0.100 None 0 1
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma
phenotype Finding 9 0.100 None 0
Reduced von Willebrand factor activity
phenotype Finding 2 1 0.100 None 0 1
CUI: C1855853
Disease: Impaired platelet aggregation
Impaired platelet aggregation
phenotype Finding 16 0.100 None 0
CUI: C0025323
Disease: Menorrhagia
Menorrhagia
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 34 6 0.100 None 0
CUI: C4025649
Disease: Reduced factor VIII activity
Reduced factor VIII activity
phenotype Finding 4 1 0.100 None 0
VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO
phenotype Finding 1 1 0.100 None 0 1
CUI: C0014591
Disease: Epistaxis
Epistaxis
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Pathologic Function 82 4 0.100 None 0
CUI: C0151563
Disease: Prolonged whole-blood clotting time
Prolonged whole-blood clotting time
phenotype Hemic and Lymphatic Diseases Finding 4 0.100 None 0
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time
phenotype Finding 39 3 0.100 None 0 1
CUI: C0042063
Disease: Urogenital Abnormalities
Urogenital Abnormalities
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 42 3 0.100 None 0
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome
disease Cardiovascular Diseases Disease or Syndrome 111 29 0.100 None 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
phenotype Finding 319 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: C0040015
Disease: Thrombasthenia
Thrombasthenia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 48 61 0.010 None 1.000 1 1982 1982
CUI: C0752143
Disease: Intracranial Thrombosis
Intracranial Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.300 None 1.000 1 1987 1987
CUI: C0752144
Disease: Brain Thrombosis
Brain Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.300 None 1.000 1 1987 1987
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 15 7 0.300 None 1.000 1 1987 1987
CUI: C0936261
Disease: Brain Thrombus
Brain Thrombus
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 1987 1987
CUI: C0936263
Disease: Cerebral Thrombus
Cerebral Thrombus
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.300 None 1.000 1 1987 1987
Extramedullary Hematopoiesis (disorder)
disease Hemic and Lymphatic Diseases Disease or Syndrome 52 1 0.010 None 1.000 1 1990 1990
CUI: C0238644
Disease: Anemia, severe
Anemia, severe
disease Hemic and Lymphatic Diseases Disease or Syndrome 65 6 0.010 None 1.000 1 1990 1990