Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0151872
Disease: Prothrombin time increased
Prothrombin time increased 		30 0 3 7.3E-02 0 0
CUI: C0019065
Disease: Hemoperitoneum
Hemoperitoneum 		1 0 1 7.1E-02 0 0
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 7.1E-02 0 0
CUI: C0266785
Disease: Abnormal umbilical cord
Abnormal umbilical cord 		1 0 1 7.1E-02 0 0
CUI: C0269608
Disease: Antepartum hemorrhage
Antepartum hemorrhage 		1 0 1 7.1E-02 0 0
CUI: C0270027
Disease: Antepartum hemorrhage affecting fetus or newborn
Antepartum hemorrhage affecting fetus or newborn 		1 0 1 7.1E-02 0 0
CUI: C0272240
Disease: Disorder of complement
Disorder of complement 		1 0 1 7.1E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 7.1E-02 0 0
CUI: C0272327
Disease: Hereditary factor X deficiency disease
Hereditary factor X deficiency disease 		1 0 1 7.1E-02 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 7.1E-02 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 7.1E-02 0 0
CUI: C0272356
Disease: von Willebrand disease, type IID
von Willebrand disease, type IID 		1 0 1 7.1E-02 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 7.1E-02 0 0
CUI: C0339815
Disease: Anterior epistaxis
Anterior epistaxis 		1 0 1 7.1E-02 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 7.1E-02 0 0
CUI: C0398610
Disease: Congenital von Willebrand's disease
Congenital von Willebrand's disease 		1 0 1 7.1E-02 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 7.1E-02 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		1 0 1 7.1E-02 0 0
CUI: C0598480
Disease: intestinal angiodysplasia
intestinal angiodysplasia 		1 0 1 7.1E-02 0 0
CUI: C0749098
Disease: Hematoma, Subdural, Acute
Hematoma, Subdural, Acute 		1 0 1 7.1E-02 0 0
CUI: C0751797
Disease: Intracranial Hematoma, Traumatic
Intracranial Hematoma, Traumatic 		1 0 1 7.1E-02 0 0
CUI: C0795843
Disease: Chromosome 12 ring
Chromosome 12 ring 		1 0 1 7.1E-02 0 0
CUI: C0865262
Disease: Thrombopathy
Thrombopathy 		1 0 1 7.1E-02 0 0
CUI: C0877456
Disease: Heyde's syndrome
Heyde's syndrome 		1 0 1 7.1E-02 0 0
CUI: C1268937
Disease: Diarrhea-negative hemolytic uremic syndrome
Diarrhea-negative hemolytic uremic syndrome 		1 0 1 7.1E-02 0 0