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: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 1.7E-03 0 0
CUI: C0043379
Disease: XYY Karyotype
XYY Karyotype 		1 0 1 1.7E-03 0 0
CUI: C0079037
Disease: Branchial Clefts-Congenital disorder
Branchial Clefts-Congenital disorder 		1 0 1 1.7E-03 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 1.7E-03 0 0
CUI: C0151905
Disease: Alanine Aminotransferase Increased
Alanine Aminotransferase Increased 		1 0 1 1.7E-03 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 1.7E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 1.7E-03 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 1.7E-03 0 0
CUI: C0153614
Disease: Malignant neoplasm of ureteric orifice
Malignant neoplasm of ureteric orifice 		1 0 1 1.7E-03 0 0
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis 		1 0 1 1.7E-03 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 1.7E-03 0 0
CUI: C0155380
Disease: Dissociated Nystagmus
Dissociated Nystagmus 		1 0 1 1.7E-03 0 0
CUI: C0155411
Disease: Exostosis of external ear canal
Exostosis of external ear canal 		1 0 1 1.7E-03 0 0
CUI: C0155747
Disease: Aneurysm of splenic artery
Aneurysm of splenic artery 		1 0 1 1.7E-03 0 0
CUI: C0155781
Disease: Thrombosed internal hemorrhoids
Thrombosed internal hemorrhoids 		1 0 1 1.7E-03 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 1.7E-03 0 0
CUI: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse 		1 0 1 1.7E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 1.7E-03 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete 		1 0 1 1.7E-03 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 1.7E-03 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 1.7E-03 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 1.7E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 1.7E-03 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 1.7E-03 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 1.7E-03 0 0