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: C1845847
Disease: Coarse facial features
Coarse facial features 		194 0 61 0.25 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		235 0 49 0.16 0 0
CUI: C0456132
Disease: Large fontanelle
Large fontanelle 		77 0 25 0.15 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 0 32 0.14 0 0
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain 		46 0 19 0.13 0 0
CUI: C0376480
Disease: Gingival Overgrowth
Gingival Overgrowth 		100 0 22 0.11 0 0
CUI: C0019825
Disease: Hoarseness
Hoarseness 		84 0 20 0.11 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 16 0.11 0 0
CUI: C0241442
Disease: Protrusion of tongue
Protrusion of tongue 		27 0 13 0.10 0 0
CUI: C0266061
Disease: Open Bite
Open Bite 		38 0 14 0.10 0 0
CUI: C0221355
Disease: Macrocephaly
Macrocephaly 		367 0 43 9.8E-02 0 0
CUI: C0426421
Disease: Wide nose
Wide nose 		87 0 18 9.8E-02 0 0
CUI: C0266298
Disease: Accessory kidney
Accessory kidney 		20 0 12 9.8E-02 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 23 9.7E-02 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		225 0 30 9.7E-02 0 0
CUI: C0432163
Disease: Defect of vertebral segmentation
Defect of vertebral segmentation 		40 0 13 9.2E-02 0 0
CUI: C0012811
Disease: Colon diverticulum anatomic structure
Colon diverticulum anatomic structure 		17 0 11 9.1E-02 0 0
CUI: C1855204
Disease: Cellular immunodeficiency
Cellular immunodeficiency 		30 0 12 9.0E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 18 9.0E-02 0 0
CUI: C0018021
Disease: Goiter
Goiter 		142 0 21 8.9E-02 0 0
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		94 0 17 8.9E-02 0 0
CUI: C0917799
Disease: Hypersomnia
Hypersomnia 		70 0 15 8.8E-02 0 0
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy 		23 0 11 8.7E-02 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		113 0 18 8.6E-02 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		417 0 42 8.6E-02 0 0