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: C4304021
Disease: Autosomal dominant macrothrombocytopenia
Autosomal dominant macrothrombocytopenia 		9 0 9 0.26 0 0
CUI: C0333864
Disease: Giant platelet (morphologic abnormality)
Giant platelet (morphologic abnormality) 		10 0 9 0.26 0 0
CUI: C2697501
Disease: Giant Platelet Count (procedure)
Giant Platelet Count (procedure) 		10 0 9 0.26 0 0
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders 		59 5 15 0.19 2 5.9E-02
CUI: C1096367
Disease: Increased mean platelet volume
Increased mean platelet volume 		10 2 7 0.19 1 3.1E-02
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time 		39 0 11 0.18 0 0
CUI: C4023154
Disease: Impaired ristocetin-induced platelet aggregation
Impaired ristocetin-induced platelet aggregation 		6 0 6 0.18 0 0
CUI: C0025323
Disease: Menorrhagia
Menorrhagia 		34 0 10 0.17 0 0
CUI: C0005129
Disease: Bernard-Soulier Syndrome
Bernard-Soulier Syndrome 		46 23 11 0.16 4 8.0E-02
CUI: C3809715
Disease: Spontaneous, recurrent epistaxis
Spontaneous, recurrent epistaxis 		11 0 6 0.15 0 0
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery 		11 0 6 0.15 0 0
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME 		42 13 10 0.15 2 4.8E-02
CUI: C1855853
Disease: Impaired platelet aggregation
Impaired platelet aggregation 		16 0 6 0.14 0 0
CUI: C1280798
Disease: Von Willebrand disease, platelet type
Von Willebrand disease, platelet type 		8 0 5 0.14 0 0
CUI: C0473237
Disease: Frank hematuria
Frank hematuria 		9 0 5 0.13 0 0
CUI: C4023026
Disease: Abnormal megakaryocyte morphology
Abnormal megakaryocyte morphology 		10 0 5 0.13 0 0
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 0 7 0.12 0 0
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		7 0 4 0.11 0 0
CUI: C2237512
Disease: cephalohematoma
cephalohematoma 		7 0 4 0.11 0 0
CUI: C1282971
Disease: von Willebrand Disease, Type 2B
von Willebrand Disease, Type 2B 		8 12 4 0.11 1 2.4E-02
CUI: C0014591
Disease: Epistaxis
Epistaxis 		82 0 11 0.10 0 0
CUI: C0272278
Disease: Congenital thrombocytopenia
Congenital thrombocytopenia 		19 0 5 0.10 0 0
CUI: C0341306
Disease: Microvillus inclusion disease
Microvillus inclusion disease 		19 0 5 0.10 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		33 0 6 9.8E-02 0 0
CUI: C0340978
Disease: May-Hegglin anomaly
May-Hegglin anomaly 		12 19 4 9.5E-02 2 4.2E-02