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: C1857280
Disease: Infra-orbital crease
Infra-orbital crease 		4 0 3 0.30 0 0
CUI: C1828017
Disease: Intermittent hyperventilation
Intermittent hyperventilation 		3 0 2 0.20 0 0
CUI: C4024917
Disease: Congenital encephalopathy
Congenital encephalopathy 		3 0 2 0.20 0 0
CUI: C0006325
Disease: Bruxism
Bruxism 		24 0 5 0.18 0 0
CUI: C0023012
Disease: Language Delay
Language Delay 		11 0 3 0.18 0 0
CUI: C0454655
Disease: Semantic-Pragmatic Disorder
Semantic-Pragmatic Disorder 		11 0 3 0.18 0 0
CUI: C0751257
Disease: Auditory Processing Disorder, Central
Auditory Processing Disorder, Central 		11 0 3 0.18 0 0
CUI: C0239154
Disease: High pitched cry
High pitched cry 		5 0 2 0.17 0 0
CUI: C1853618
Disease: Perivascular spaces
Perivascular spaces 		5 0 2 0.17 0 0
CUI: C0576227
Disease: Narrow foot
Narrow foot 		6 0 2 0.15 0 0
CUI: C4024167
Disease: Abnormality of the antitragus
Abnormality of the antitragus 		7 0 2 0.14 0 0
CUI: C4022908
Disease: Cerebral white matter hypoplasia
Cerebral white matter hypoplasia 		8 0 2 0.13 0 0
CUI: C0023014
Disease: Language Development Disorders
Language Development Disorders 		18 0 3 0.12 0 0
CUI: C0677608
Disease: Chorioangioma
Chorioangioma 		9 0 2 0.12 0 0
CUI: C0265220
Disease: Pallister-Hall syndrome
Pallister-Hall syndrome 		10 0 2 0.12 0 0
CUI: C1833362
Disease: Sleep-wake cycle disturbance
Sleep-wake cycle disturbance 		10 0 2 0.12 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 0.11 0 0
CUI: C0020578
Disease: Hyperventilation
Hyperventilation 		31 0 4 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: C0038131
Disease: Stammering
Stammering 		1 0 1 0.11 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 0.11 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 0.11 0 0
CUI: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome 		11 0 2 0.11 0 0