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: C1096250
Disease: Gastrointestinal discomfort
Gastrointestinal discomfort 		4 0 3 0.30 0 0
CUI: C0795833
Disease: KLEEFSTRA SYNDROME 1
KLEEFSTRA SYNDROME 1 		9 0 3 0.20 0 0
CUI: C4551771
Disease: Kleefstra syndrome
Kleefstra syndrome 		9 0 3 0.20 0 0
CUI: C3495890
Disease: Osteochondral defects
Osteochondral defects 		17 0 3 0.13 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 0.11 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 0.11 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 0.11 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 0.11 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 0.11 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 0.11 0 0
CUI: C0477729
Disease: Other chronic tubulo-interstitial nephritis
Other chronic tubulo-interstitial nephritis 		1 0 1 0.11 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 0.11 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 0.11 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 0.11 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 0.11 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 0.11 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 0.11 0 0
CUI: C1392616
Disease: Nonobstructive chronic pyelonephritis NOS
Nonobstructive chronic pyelonephritis NOS 		1 0 1 0.11 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 0.11 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 0.11 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 0.11 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 0 1 0.11 0 0
CUI: C1867332
Disease: Reticular Dystrophy Of Retinal Pigment Epithelium
Reticular Dystrophy Of Retinal Pigment Epithelium 		1 0 1 0.11 0 0
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 0 1 0.11 0 0
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79 		1 0 1 0.11 0 0