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: C0038449
Disease: Stricture of artery
Stricture of artery 		16 0 4 9.3E-02 0 0
CUI: C1856872
Disease: Down-sloping shoulders
Down-sloping shoulders 		32 0 5 8.6E-02 0 0
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome 		20 0 4 8.5E-02 0 0
CUI: C0034089
Disease: Pulmonary Valve Stenosis
Pulmonary Valve Stenosis 		16 0 3 6.8E-02 0 0
CUI: C0270972
Disease: Cornelia De Lange Syndrome
Cornelia De Lange Syndrome 		48 0 5 6.8E-02 0 0
CUI: C0156273
Disease: Bladder Diverticulum
Bladder Diverticulum 		18 0 3 6.5E-02 0 0
CUI: C0266015
Disease: Congenital digestive system anomalies
Congenital digestive system anomalies 		2 5 2 6.5E-02 2 7.4E-02
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant 		3 0 2 6.2E-02 0 0
CUI: C0406549
Disease: Cutis laxa, acquired type
Cutis laxa, acquired type 		3 0 2 6.2E-02 0 0
CUI: C3276744
Disease: Absent tibia
Absent tibia 		3 0 2 6.2E-02 0 0
CUI: C4020949
Disease: Abnormal emotion/affect behavior
Abnormal emotion/affect behavior 		3 13 2 6.2E-02 6 0.19
CUI: C3501846
Disease: Noonan-Like Syndrome With Loose Anagen Hair
Noonan-Like Syndrome With Loose Anagen Hair 		22 0 3 6.0E-02 0 0
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis 		23 0 3 5.9E-02 0 0
CUI: C0263428
Disease: Burnett Schwartz Berberian syndrome
Burnett Schwartz Berberian syndrome 		5 0 2 5.9E-02 0 0
CUI: C1395674
Disease: Bowel diverticulosis
Bowel diverticulosis 		5 0 2 5.9E-02 0 0
CUI: C1864796
Disease: Pectus excavatum of inferior sternum
Pectus excavatum of inferior sternum 		5 0 2 5.9E-02 0 0
CUI: C4020740
Disease: Clinodactyly of the 4th toe
Clinodactyly of the 4th toe 		5 0 2 5.9E-02 0 0
CUI: C1834120
Disease: NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME (disorder)
NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME (disorder) 		6 0 2 5.7E-02 0 0
CUI: C0031391
Disease: Phencyclidine Abuse
Phencyclidine Abuse 		7 0 2 5.6E-02 0 0
CUI: C0234398
Disease: Visual Cortex Disorder
Visual Cortex Disorder 		7 0 2 5.6E-02 0 0
CUI: C0236742
Disease: Phencyclidine-Related Disorders
Phencyclidine-Related Disorders 		7 0 2 5.6E-02 0 0
CUI: C0266623
Disease: Congenital anomaly of neck
Congenital anomaly of neck 		26 0 3 5.6E-02 0 0
CUI: C1857126
Disease: Parietal bossing
Parietal bossing 		7 0 2 5.6E-02 0 0
CUI: C4025749
Disease: Abnormality of the spleen
Abnormality of the spleen 		26 0 3 5.6E-02 0 0
CUI: C1860493
Disease: Abnormality of the sternum
Abnormality of the sternum 		46 11 4 5.5E-02 2 6.1E-02