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: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
96 0 17 0.13 0 0
CUI: C1844505
Disease: Pointed chin
Pointed chin
71 0 14 0.13 0 0
CUI: C0156273
Disease: Bladder Diverticulum
Bladder Diverticulum
18 0 8 0.13 0 0
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain
46 0 11 0.12 0 0
CUI: C0034880
Disease: Hyperacusis
Hyperacusis
20 0 8 0.12 0 0
CUI: C0080174
Disease: Spina Bifida Occulta
Spina Bifida Occulta
76 0 14 0.12 0 0
CUI: C4023676
Disease: Increased nuchal translucency
Increased nuchal translucency
30 0 9 0.12 0 0
CUI: C0151205
Disease: Periorbital edema
Periorbital edema
22 0 8 0.12 0 0
CUI: C4553313
Disease: Periorbital Edema, CTCAE
Periorbital Edema, CTCAE
22 0 8 0.12 0 0
CUI: C1856872
Disease: Down-sloping shoulders
Down-sloping shoulders
32 0 9 0.12 0 0
CUI: C0018536
Disease: Hallux Valgus
Hallux Valgus
61 0 12 0.12 0 0
CUI: C4021662
Disease: Abnormal endocardium morphology
Abnormal endocardium morphology
23 0 8 0.12 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality
23 0 8 0.12 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris
52 0 11 0.12 0 0
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
35 0 9 0.11 0 0
Abnormality of pelvic girdle bone morphology
55 0 11 0.11 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus
46 0 10 0.11 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 24 11 0.11 2 7.7E-02
CUI: C0578626
Disease: blue iris (physical finding)
blue iris (physical finding)
28 0 8 0.11 0 0
CUI: C0040588
Disease: Tracheoesophageal Fistula
Tracheoesophageal Fistula
80 0 13 0.11 0 0
CUI: C4021801
Disease: Lacrimation abnormality
Lacrimation abnormality
29 0 8 0.11 0 0
CUI: C1837279
Disease: Hypoplastic toenails
Hypoplastic toenails
42 0 9 0.10 0 0
CUI: C0234144
Disease: Dysgraphia
Dysgraphia
43 0 9 0.10 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon
44 0 9 0.10 0 0
CUI: C0034888
Disease: Rectal Prolapse
Rectal Prolapse
46 0 9 1.0E-01 0 0