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: C0855999
Disease: Abnormal eosinophil morphology
Abnormal eosinophil morphology 		3 0 1 0.17 0 0
CUI: C1096368
Disease: Decreased mean platelet volume
Decreased mean platelet volume 		3 0 1 0.17 0 0
CUI: C1282974
Disease: von Willebrand disease type 2M
von Willebrand disease type 2M 		3 0 1 0.17 0 0
CUI: C1866032
Disease: Honeycomb palmoplantar keratoderma
Honeycomb palmoplantar keratoderma 		3 0 1 0.17 0 0
CUI: C2713537
Disease: Deficiency of Platelet Glycoprotein 1b
Deficiency of Platelet Glycoprotein 1b 		3 0 1 0.17 0 0
CUI: C4023150
Disease: Decreased platelet glycoprotein Ib-IX-V
Decreased platelet glycoprotein Ib-IX-V 		3 0 1 0.17 0 0
CUI: C0236175
Disease: Increased IgE level
Increased IgE level 		4 6 1 0.14 1 0.17
CUI: C0854145
Disease: Feeding Disorders
Feeding Disorders 		4 0 1 0.14 0 0
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		4 0 1 0.14 0 0
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		4 0 1 0.14 0 0
CUI: C3826102
Disease: Iron deficiency anemia in children
Iron deficiency anemia in children 		4 0 1 0.14 0 0
CUI: C4024630
Disease: Partially duplicated kidney
Partially duplicated kidney 		4 0 1 0.14 0 0
CUI: C0020058
Disease: Howell-Jolly Bodies
Howell-Jolly Bodies 		5 0 1 0.12 0 0
CUI: C1839305
Disease: Decreased proportion of CD8-positive T cells
Decreased proportion of CD8-positive T cells 		5 1 1 0.12 1 1.00
CUI: C0151683
Disease: Neutrophilia (finding)
Neutrophilia (finding) 		6 1 1 0.11 1 1.00
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 0 1 0.11 0 0
CUI: C0343755
Disease: HIV Wasting Syndrome
HIV Wasting Syndrome 		6 0 1 0.11 0 0
CUI: C1527388
Disease: Amniotic Bands
Amniotic Bands 		6 0 1 0.11 0 0
CUI: C4021747
Disease: Specific anti-polysaccharide antibody deficiency
Specific anti-polysaccharide antibody deficiency 		6 0 1 0.11 0 0
CUI: C4023154
Disease: Impaired ristocetin-induced platelet aggregation
Impaired ristocetin-induced platelet aggregation 		6 0 1 0.11 0 0
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		7 0 1 1.0E-01 0 0
CUI: C0162679
Disease: Leukemic Infiltration
Leukemic Infiltration 		7 0 1 1.0E-01 0 0
CUI: C2237512
Disease: cephalohematoma
cephalohematoma 		7 0 1 1.0E-01 0 0
CUI: C3805919
Disease: Recurrent intrapulmonary hemorrhage
Recurrent intrapulmonary hemorrhage 		7 0 1 1.0E-01 0 0
CUI: C3844293
Disease: Oval fat body
Oval fat body 		7 0 1 1.0E-01 0 0