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: C0085697
Disease: Chronic pyelonephritis
Chronic pyelonephritis 		1 0 1 0.50 0 0
CUI: C0749393
Disease: Chronic thrombocytopenia
Chronic thrombocytopenia 		1 0 1 0.50 0 0
CUI: C1879691
Disease: Amegakaryocytosis
Amegakaryocytosis 		1 0 1 0.50 0 0
CUI: C2586012
Disease: Hereditary thrombocytopenic disorder
Hereditary thrombocytopenic disorder 		1 0 1 0.50 0 0
CUI: C3280114
Disease: Glycoprotein IA Deficiency
Glycoprotein IA Deficiency 		1 0 1 0.50 0 0
CUI: C0948968
Disease: Osteomyelofibrosis
Osteomyelofibrosis 		2 0 1 0.33 0 0
CUI: C2931757
Disease: Acquired amegakaryocytic thrombocytopenia
Acquired amegakaryocytic thrombocytopenia 		2 0 1 0.33 0 0
CUI: C0235604
Disease: Qualitative platelet deficiency
Qualitative platelet deficiency 		3 0 1 0.25 0 0
CUI: C4273671
Disease: Inherited predisposition to essential thrombocythemia
Inherited predisposition to essential thrombocythemia 		3 0 1 0.25 0 0
CUI: C0154301
Disease: Acquired thrombocytopenia
Acquired thrombocytopenia 		4 0 1 0.20 0 0
CUI: C0854866
Disease: Recurrent Non-Hodgkin Lymphoma
Recurrent Non-Hodgkin Lymphoma 		4 0 1 0.20 0 0
CUI: C1527411
Disease: Thrombosis of retinal vein
Thrombosis of retinal vein 		4 0 1 0.20 0 0
CUI: C0272296
Disease: Thrombocytopenia due to sequestration
Thrombocytopenia due to sequestration 		5 0 1 0.17 0 0
CUI: C3277671
Disease: THROMBOCYTHEMIA 1
THROMBOCYTHEMIA 1 		5 0 1 0.17 0 0
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		7 0 1 0.12 0 0
CUI: C1327915
Disease: Congenital amegakaryocytic thrombocytopenia
Congenital amegakaryocytic thrombocytopenia 		7 0 1 0.12 0 0
CUI: C2237512
Disease: cephalohematoma
cephalohematoma 		7 0 1 0.12 0 0
CUI: C4303761
Disease: Familial thrombocytosis
Familial thrombocytosis 		7 0 1 0.12 0 0
CUI: C0457506
Disease: Reactive thrombocytosis
Reactive thrombocytosis 		9 0 1 1.0E-01 0 0
CUI: C3489628
Disease: Thrombocytosis, Autosomal Dominant
Thrombocytosis, Autosomal Dominant 		9 0 1 1.0E-01 0 0
CUI: C0741250
Disease: aspirin sensitivity
aspirin sensitivity 		10 0 1 9.1E-02 0 0
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		10 0 1 9.1E-02 0 0
CUI: C0175703
Disease: Thrombocytopenia-Absent Radius Syndrome
Thrombocytopenia-Absent Radius Syndrome 		12 0 1 7.7E-02 0 0
CUI: C3854603
Disease: FNAITP
FNAITP 		12 0 1 7.7E-02 0 0
CUI: C0025222
Disease: Melena
Melena 		15 0 1 6.2E-02 0 0