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: C4023145
Disease: Abnormal umbilical stump bleeding
Abnormal umbilical stump bleeding 		disease Anatomical Abnormality 5 0.100 None 0
CUI: C4016042
Disease: VENOUS THROMBOSIS, SUSCEPTIBILITY TO
VENOUS THROMBOSIS, SUSCEPTIBILITY TO 		phenotype Finding 1 0.300 strong 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: C3279439
Disease: Recurrent spontaneous abortion
Recurrent spontaneous abortion 		phenotype Female Urogenital Diseases and Pregnancy Complications Finding 7 0.100 None 0
CUI: C4022608
Disease: Oral cavity bleeding
Oral cavity bleeding 		phenotype Pathologic Function 18 0.100 None 0
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma 		phenotype Finding 9 0.100 None 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		disease Disease or Syndrome 33 0.100 None 0
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: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Pathologic Function 50 2 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: C0023470
Disease: Myeloid Leukemia
Myeloid Leukemia 		disease Neoplasms Neoplastic Process 385 7 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: C0032797
Disease: Postpartum Hemorrhage
Postpartum Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 6 0.100 None 0
CUI: C0085605
Disease: Liver Failure
Liver Failure 		disease Digestive System Diseases Disease or Syndrome 293 20 0.100 None 0
CUI: C0269855
Disease: Hematoma of cord
Hematoma of cord 		phenotype Pathological Conditions, Signs and Symptoms Injury or Poisoning 2 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: C0578878
Disease: Inflammation of large intestine
Inflammation of large intestine 		phenotype Digestive System Diseases Disease or Syndrome 12 1 0.100 None 0
CUI: C0240412
Disease: Muscle hematoma
Muscle hematoma 		disease Pathological Conditions, Signs and Symptoms Injury or Poisoning 6 0.100 None 0
CUI: C0013491
Disease: Ecchymosis
Ecchymosis 		phenotype Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Pathologic Function 41 2 0.100 None 0
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1800 680 0.020 None 1.000 2 1 2003 2007
CUI: C2750481
Disease: Factor XIII, B Subunit, Deficiency Of
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: 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