F13B, coagulation factor XIII B chain, 2165

N. diseases: 47; N. variants: 23
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: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
phenotype Laboratory Procedure 55 427 0.100 None 1.000 1 15 2013 2013
CUI: C4511230
Disease: Bathing suit ichthyosis
Bathing suit ichthyosis
disease Disease or Syndrome 3 1 0.010 None 1.000 1 2006 2006
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas
disease Disease or Syndrome 33 0.100 None 0
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma
phenotype Finding 9 0.100 None 0
CUI: C1851789
Disease: Poor wound healing
Poor wound healing
phenotype Finding 19 3 0.100 None 0
Prolonged bleeding after dental extraction
phenotype Pathologic Function 8 0.100 None 0
VENOUS THROMBOSIS, SUSCEPTIBILITY TO
phenotype Finding 1 0.300 strong 0
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery
phenotype Pathologic Function 11 0.100 None 0
CUI: C4022608
Disease: Oral cavity bleeding
Oral cavity bleeding
phenotype Pathologic Function 18 0.100 None 0
Prolonged bleeding following circumcision
phenotype Pathologic Function 5 0.100 None 0
CUI: C4023143
Disease: Bleeding with minor or no trauma
Bleeding with minor or no trauma
phenotype Pathologic Function 3 0.100 None 0
CUI: C4023145
Disease: Abnormal umbilical stump bleeding
Abnormal umbilical stump bleeding
disease Anatomical Abnormality 5 0.100 None 0
CUI: C4024692
Disease: Reduced factor XIII activity
Reduced factor XIII activity
phenotype Finding 5 0.100 None 0
CUI: C4280712
Disease: Delayed onset bleeding
Delayed onset bleeding
phenotype Pathologic Function 2 0.100 None 0
CUI: C0042345
Disease: Varicosity
Varicosity
disease Cardiovascular Diseases Disease or Syndrome 188 51 0.010 None 1.000 1 1991 1991
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 117 218 0.300 None 1.000 1 2005 2005
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
disease Cardiovascular Diseases Disease or Syndrome 230 93 0.300 None 1.000 1 2005 2005
Factor XIII, B Subunit, Deficiency Of
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Finding 1 7 0.700 strong 1.000 4 7 1993 2015
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 10 4 0.600 strong 1.000 2 1990 2011
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome 978 115 0.010 None 1.000 1 2002 2002
CUI: C0085605
Disease: Liver Failure
Liver Failure
disease Digestive System Diseases Disease or Syndrome 293 20 0.100 None 0
CUI: C0578878
Disease: Inflammation of large intestine
Inflammation of large intestine
phenotype Digestive System Diseases Disease or Syndrome 12 1 0.100 None 0
CUI: C3279439
Disease: Recurrent spontaneous abortion
Recurrent spontaneous abortion
phenotype Female Urogenital Diseases and Pregnancy Complications Finding 7 0.100 None 0
CUI: C0016085
Disease: Filariasis
Filariasis
disease Infections Disease or Syndrome 32 0.010 None 1.000 1 2004 2004
CUI: C0392663
Disease: Infection by Wuchereria bancrofti
Infection by Wuchereria bancrofti
disease Infections; Hemic and Lymphatic Diseases Disease or Syndrome 9 2 0.010 None 1.000 1 2004 2004