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: C0085650
Disease: Purpura Fulminans
Purpura Fulminans 		15 1 7 0.30 1 0.50
CUI: C0024248
Disease: Lymphocele
Lymphocele 		5 0 4 0.25 0 0
CUI: C0742857
Disease: Acute cough
Acute cough 		6 0 4 0.24 0 0
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 1 8 0.22 1 0.50
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		3 0 3 0.20 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 0 6 0.19 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 3 0.18 0 0
CUI: C1868251
Disease: Neonatal alloimmune thrombocytopenia (NAIT)
Neonatal alloimmune thrombocytopenia (NAIT) 		6 0 3 0.17 0 0
CUI: C0333864
Disease: Giant platelet (morphologic abnormality)
Giant platelet (morphologic abnormality) 		10 0 3 0.14 0 0
CUI: C2697501
Disease: Giant Platelet Count (procedure)
Giant Platelet Count (procedure) 		10 0 3 0.14 0 0
CUI: C0340704
Disease: Superior mesenteric vein thrombosis
Superior mesenteric vein thrombosis 		2 0 2 0.13 0 0
CUI: C1867638
Disease: Warfarin-induced skin necrosis
Warfarin-induced skin necrosis 		2 0 2 0.13 0 0
CUI: C2930896
Disease: Congenital thrombotic disease, due to Protein C deficiency
Congenital thrombotic disease, due to Protein C deficiency 		2 0 2 0.13 0 0
CUI: C0270500
Disease: Coprophilia (disorder)
Coprophilia (disorder) 		12 0 3 0.12 0 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		3 0 2 0.12 0 0
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		13 0 3 0.12 0 0
CUI: C0478019
Disease: Other specified congenital malformations of respiratory system
Other specified congenital malformations of respiratory system 		13 0 3 0.12 0 0
CUI: C2363755
Disease: Acquired Protein S Deficiency
Acquired Protein S Deficiency 		4 0 2 0.12 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 3 0.12 0 0
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 0 6 0.12 0 0
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		35 0 5 0.11 0 0
CUI: C4025100
Disease: Abnormal respiratory motile cilium morphology
Abnormal respiratory motile cilium morphology 		5 0 2 0.11 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 2 0.11 0 0
CUI: C4023154
Disease: Impaired ristocetin-induced platelet aggregation
Impaired ristocetin-induced platelet aggregation 		6 0 2 0.11 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 0 3 0.10 0 0