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: C1860614
Disease: ULNAR HYPOPLASIA
ULNAR HYPOPLASIA 		50 0 24 0.16 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx 		23 0 20 0.16 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 0 27 0.16 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney 		40 0 22 0.16 0 0
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		40 0 22 0.16 0 0
CUI: C0266387
Disease: Bicornuate uterus
Bicornuate uterus 		44 0 22 0.15 0 0
CUI: C2749463
Disease: Aplasia/Hypoplasia of the radius
Aplasia/Hypoplasia of the radius 		45 0 22 0.15 0 0
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		95 0 28 0.15 0 0
CUI: C0263498
Disease: Premature canities
Premature canities 		33 0 20 0.15 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 22 0.14 0 0
CUI: C4025819
Disease: Abnormality of the hypothalamus-pituitary axis
Abnormality of the hypothalamus-pituitary axis 		70 0 24 0.14 0 0
CUI: C1855204
Disease: Cellular immunodeficiency
Cellular immunodeficiency 		30 0 19 0.14 0 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction 		87 0 26 0.14 0 0
CUI: C0423112
Disease: Short palpebral fissure
Short palpebral fissure 		91 0 26 0.14 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism 		92 0 26 0.14 0 0
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		76 0 24 0.14 0 0
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		137 0 31 0.14 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 22 0.13 0 0
CUI: C0521620
Disease: Dilatation of ureter
Dilatation of ureter 		72 0 23 0.13 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology 		30 0 18 0.13 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		175 0 35 0.13 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		175 0 35 0.13 0 0
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule 		59 0 21 0.13 0 0
CUI: C1857453
Disease: Renal hypoplasia/aplasia
Renal hypoplasia/aplasia 		73 0 22 0.13 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 32 0.12 0 0