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: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		34 0 10 0.10 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 8 1.0E-01 0 0
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 8 1.0E-01 0 0
CUI: C0221209
Disease: Pelvic kidney
Pelvic kidney 		15 0 8 9.9E-02 0 0
CUI: C0795949
Disease: Galloway Mowat syndrome
Galloway Mowat syndrome 		15 0 8 9.9E-02 0 0
CUI: C0018536
Disease: Hallux Valgus
Hallux Valgus 		61 0 12 9.8E-02 0 0
CUI: C4025660
Disease: Abnormality of the ankles
Abnormality of the ankles 		17 0 8 9.6E-02 0 0
CUI: C4021801
Disease: Lacrimation abnormality
Lacrimation abnormality 		29 0 9 9.6E-02 0 0
CUI: C0156273
Disease: Bladder Diverticulum
Bladder Diverticulum 		18 0 8 9.5E-02 0 0
CUI: C0751466
Disease: Phonophobia
Phonophobia 		18 0 8 9.5E-02 0 0
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		42 0 10 9.4E-02 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 11 9.3E-02 0 0
CUI: C0034880
Disease: Hyperacusis
Hyperacusis 		20 0 8 9.3E-02 0 0
CUI: C0266298
Disease: Accessory kidney
Accessory kidney 		20 0 8 9.3E-02 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 22 9.2E-02 0 0
CUI: C0151205
Disease: Periorbital edema
Periorbital edema 		22 0 8 9.1E-02 0 0
CUI: C4553313
Disease: Periorbital Edema, CTCAE
Periorbital Edema, CTCAE 		22 0 8 9.1E-02 0 0
CUI: C0345030
Disease: Peripheral pulmonary artery stenosis
Peripheral pulmonary artery stenosis 		23 0 8 9.0E-02 0 0
CUI: C1843517
Disease: Retinal arteriolar tortuosity
Retinal arteriolar tortuosity 		23 0 8 9.0E-02 0 0
CUI: C4021662
Disease: Abnormal endocardium morphology
Abnormal endocardium morphology 		23 0 8 9.0E-02 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality 		23 0 8 9.0E-02 0 0
CUI: C0581342
Disease: Redundant skin
Redundant skin 		48 0 10 8.9E-02 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		123 10 16 8.8E-02 2 0.15
CUI: C0265224
Disease: Freeman-Sheldon syndrome
Freeman-Sheldon syndrome 		26 0 8 8.7E-02 0 0
CUI: C0266623
Disease: Congenital anomaly of neck
Congenital anomaly of neck 		26 0 8 8.7E-02 0 0