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: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia 		1 0 1 1.2E-02 0 0
CUI: C0018814
Disease: Heart Rupture, Post-Infarction
Heart Rupture, Post-Infarction 		1 0 1 1.2E-02 0 0
CUI: C0019065
Disease: Hemoperitoneum
Hemoperitoneum 		1 0 1 1.2E-02 0 0
CUI: C0019640
Disease: Histomoniasis
Histomoniasis 		1 0 1 1.2E-02 0 0
CUI: C0026471
Disease: Monoclonal paraproteinemia
Monoclonal paraproteinemia 		1 0 1 1.2E-02 0 0
CUI: C0029163
Disease: Oral Hemorrhage
Oral Hemorrhage 		1 0 1 1.2E-02 0 0
CUI: C0029804
Disease: Other specified hemorrhagic conditions
Other specified hemorrhagic conditions 		1 0 1 1.2E-02 0 0
CUI: C0037974
Disease: Spirochaetales Infections
Spirochaetales Infections 		1 0 1 1.2E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 1.2E-02 0 0
CUI: C0152092
Disease: Juvenile dermatitis herpetiformis
Juvenile dermatitis herpetiformis 		1 0 1 1.2E-02 0 0
CUI: C0152902
Disease: Tuberculosis of esophagus
Tuberculosis of esophagus 		1 0 1 1.2E-02 0 0
CUI: C0153888
Disease: Chronic myeloid leukemia in remission
Chronic myeloid leukemia in remission 		1 0 1 1.2E-02 0 0
CUI: C0162637
Disease: Strongylida Infections
Strongylida Infections 		1 0 1 1.2E-02 0 0
CUI: C0234959
Disease: Panarteritis
Panarteritis 		1 0 1 1.2E-02 0 0
CUI: C0266785
Disease: Abnormal umbilical cord
Abnormal umbilical cord 		1 0 1 1.2E-02 0 0
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		1 0 1 1.2E-02 0 0
CUI: C0267827
Disease: Acute toxic hepatitis
Acute toxic hepatitis 		1 0 1 1.2E-02 0 0
CUI: C0268757
Disease: SLE glomerulonephritis syndrome, WHO class IV
SLE glomerulonephritis syndrome, WHO class IV 		1 0 1 1.2E-02 0 0
CUI: C0269608
Disease: Antepartum hemorrhage
Antepartum hemorrhage 		1 0 1 1.2E-02 0 0
CUI: C0270027
Disease: Antepartum hemorrhage affecting fetus or newborn
Antepartum hemorrhage affecting fetus or newborn 		1 0 1 1.2E-02 0 0
CUI: C0270805
Disease: Hemiplegic cerebral palsy
Hemiplegic cerebral palsy 		1 0 1 1.2E-02 0 0
CUI: C0272272
Disease: Systemic fibrinogenolysis
Systemic fibrinogenolysis 		1 0 1 1.2E-02 0 0
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		1 0 1 1.2E-02 0 0
CUI: C0272282
Disease: Thrombocytopenia, cyclic
Thrombocytopenia, cyclic 		1 0 1 1.2E-02 0 0
CUI: C0272327
Disease: Hereditary factor X deficiency disease
Hereditary factor X deficiency disease 		1 0 1 1.2E-02 0 0