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: C1837650
Disease: Lack of spontaneous play
Lack of spontaneous play 		5 0 3 0.60 0 0
CUI: C1837653
Disease: Inflexible adherence to routines or rituals
Inflexible adherence to routines or rituals 		5 0 3 0.60 0 0
CUI: C1837649
Disease: Impaired ability to form peer relationships
Impaired ability to form peer relationships 		3 0 2 0.50 0 0
CUI: C0877243
Disease: Increased serum serotonin
Increased serum serotonin 		8 0 3 0.38 0 0
CUI: C4021798
Disease: Impaired use of nonverbal behaviors
Impaired use of nonverbal behaviors 		8 0 3 0.38 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 0.33 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 0.33 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 0.33 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 0.33 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 0.33 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 0.33 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 0.33 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 0.33 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 0.33 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 0.33 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 0.33 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 0.33 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 0.33 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 0.33 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 0.33 0 0
CUI: C1845334
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		1 0 1 0.33 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 0 1 0.33 0 0
CUI: C1845341
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) 		1 0 1 0.33 0 0
CUI: C1845539
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		1 0 1 0.33 0 0
CUI: C1845540
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding) 		1 0 1 0.33 0 0