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: C0014394
Disease: Enuresis
Enuresis 		0 3 0 0 1 3.4E-02
CUI: C0241521
Disease: Ulnar deviation of hand
Ulnar deviation of hand 		0 2 0 0 1 3.6E-02
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		0 16 0 0 1 2.4E-02
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		0 19 0 0 1 2.2E-02
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		0 10 0 0 1 2.8E-02
CUI: C1306587
Disease: Acute encephalopathy
Acute encephalopathy 		0 3 0 0 1 3.4E-02
CUI: C1836038
Disease: Poor head control
Poor head control 		0 13 0 0 1 2.6E-02
CUI: C1836696
Disease: Lower limb hyperreflexia
Lower limb hyperreflexia 		0 6 0 0 1 3.1E-02
CUI: C1963101
Disease: Encephalopathy, CTCAE 3.0
Encephalopathy, CTCAE 3.0 		0 24 0 0 1 2.0E-02
CUI: C4023077
Disease: EEG with central focal spikes
EEG with central focal spikes 		0 2 0 0 1 3.6E-02
CUI: C4023353
Disease: Abnormality of coordination
Abnormality of coordination 		0 3 0 0 1 3.4E-02
CUI: C4025792
Disease: EEG with irregular generalized spike and wave complexes
EEG with irregular generalized spike and wave complexes 		0 1 0 0 1 3.7E-02
CUI: C4317045
Disease: Gluten intolerance
Gluten intolerance 		0 1 0 0 1 3.7E-02
CUI: C4693362
Disease: EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2
EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2 		0 7 0 0 1 3.0E-02
CUI: C0016512
Disease: Foot pain
Foot pain 		1 0 1 4.5E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 1 1 4.5E-02 1 3.7E-02
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 4.5E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 4.5E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 4.5E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 4.5E-02 0 0
CUI: C0268371
Disease: Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails 		1 0 1 4.5E-02 0 0
CUI: C0405124
Disease: Nuchal Cord
Nuchal Cord 		1 1 1 4.5E-02 1 3.7E-02
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 4.5E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 0 1 4.5E-02 0 0
CUI: C0474886
Disease: Localized recessive dystrophic epidermolysis bullosa
Localized recessive dystrophic epidermolysis bullosa 		1 0 1 4.5E-02 0 0