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: C0020875
Disease: Ileal Diseases
Ileal Diseases 		0 7 0 0 1 5.9E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		234 0 1 2.3E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 2.5E-03 0 0
CUI: C0424678
Disease: Lean body mass
Lean body mass 		144 0 1 3.0E-03 0 0
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		134 0 1 3.1E-03 0 0
CUI: C0029443
Disease: Osteomyelitis
Osteomyelitis 		121 0 1 3.2E-03 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 0 1 3.3E-03 0 0
CUI: C3160909
Disease: Autoimmune arthritis
Autoimmune arthritis 		113 0 1 3.3E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 0 1 3.3E-03 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 1 3.3E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 3.3E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		104 0 1 3.4E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 3.4E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 3.4E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 3.4E-03 0 0
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification 		103 0 1 3.4E-03 0 0
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		100 0 1 3.4E-03 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia 		100 0 1 3.4E-03 0 0
CUI: C0919747
Disease: Cytokine storm
Cytokine storm 		97 0 1 3.4E-03 0 0
CUI: C0687120
Disease: Nephronophthisis
Nephronophthisis 		96 0 1 3.5E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 3.5E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 4 1 3.5E-03 2 0.15
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 1 3.5E-03 0 0
CUI: C0349632
Disease: Splenic Marginal Zone B-Cell Lymphoma
Splenic Marginal Zone B-Cell Lymphoma 		93 0 1 3.5E-03 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		92 0 1 3.5E-03 0 0