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: C4087502
Disease: Giant platelet disorder
Giant platelet disorder 		1 0 1 0.50 0 0
CUI: C2713537
Disease: Deficiency of Platelet Glycoprotein 1b
Deficiency of Platelet Glycoprotein 1b 		3 0 1 0.25 0 0
CUI: C4023150
Disease: Decreased platelet glycoprotein Ib-IX-V
Decreased platelet glycoprotein Ib-IX-V 		3 0 1 0.25 0 0
CUI: C1096367
Disease: Increased mean platelet volume
Increased mean platelet volume 		10 2 2 0.20 1 0.33
CUI: C4024630
Disease: Partially duplicated kidney
Partially duplicated kidney 		4 0 1 0.20 0 0
CUI: C4023154
Disease: Impaired ristocetin-induced platelet aggregation
Impaired ristocetin-induced platelet aggregation 		6 0 1 0.14 0 0
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		7 0 1 0.12 0 0
CUI: C2237512
Disease: cephalohematoma
cephalohematoma 		7 0 1 0.12 0 0
CUI: C1969572
Disease: Prolonged bleeding after dental extraction
Prolonged bleeding after dental extraction 		8 0 1 0.11 0 0
CUI: C0473237
Disease: Frank hematuria
Frank hematuria 		9 0 1 1.0E-01 0 0
CUI: C4024912
Disease: Occipital myelomeningocele
Occipital myelomeningocele 		9 0 1 1.0E-01 0 0
CUI: C4304021
Disease: Autosomal dominant macrothrombocytopenia
Autosomal dominant macrothrombocytopenia 		9 0 1 1.0E-01 0 0
CUI: C0333864
Disease: Giant platelet (morphologic abnormality)
Giant platelet (morphologic abnormality) 		10 0 1 9.1E-02 0 0
CUI: C2697501
Disease: Giant Platelet Count (procedure)
Giant Platelet Count (procedure) 		10 0 1 9.1E-02 0 0
CUI: C4023026
Disease: Abnormal megakaryocyte morphology
Abnormal megakaryocyte morphology 		10 0 1 9.1E-02 0 0
CUI: C3809715
Disease: Spontaneous, recurrent epistaxis
Spontaneous, recurrent epistaxis 		11 0 1 8.3E-02 0 0
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery 		11 0 1 8.3E-02 0 0
CUI: C0340978
Disease: May-Hegglin anomaly
May-Hegglin anomaly 		12 0 1 7.7E-02 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome 		12 0 1 7.7E-02 0 0
CUI: C3854603
Disease: FNAITP
FNAITP 		12 0 1 7.7E-02 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis 		12 0 1 7.7E-02 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils 		12 0 1 7.7E-02 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch 		13 0 1 7.1E-02 0 0
CUI: C0018926
Disease: Hematemesis
Hematemesis 		14 0 1 6.7E-02 0 0
CUI: C0025222
Disease: Melena
Melena 		15 0 1 6.2E-02 0 0