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: C1845341
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) 		1 1 1 1.00 1 1.00
CUI: C0426317
Disease: Genitourinary symptoms
Genitourinary symptoms 		2 1 1 0.50 1 1.00
CUI: C1837649
Disease: Impaired ability to form peer relationships
Impaired ability to form peer relationships 		3 0 1 0.33 0 0
CUI: C1845337
Disease: Lack of peer relationships
Lack of peer relationships 		3 0 1 0.33 0 0
CUI: C1837650
Disease: Lack of spontaneous play
Lack of spontaneous play 		5 0 1 0.20 0 0
CUI: C1837653
Disease: Inflexible adherence to routines or rituals
Inflexible adherence to routines or rituals 		5 0 1 0.20 0 0
CUI: C0877243
Disease: Increased serum serotonin
Increased serum serotonin 		8 0 1 0.12 0 0
CUI: C4021798
Disease: Impaired use of nonverbal behaviors
Impaired use of nonverbal behaviors 		8 0 1 0.12 0 0
CUI: C4726566
Disease: Extracranial Solid Neoplasm
Extracranial Solid Neoplasm 		8 0 1 0.12 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior 		13 0 1 7.7E-02 0 0
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		16 6 1 6.2E-02 1 0.17
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder 		40 4 1 2.5E-02 1 0.25
CUI: C1837352
Disease: Childhood onset
Childhood onset 		56 0 1 1.8E-02 0 0
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		69 0 1 1.4E-02 0 0
CUI: C2986658
Disease: Diffuse Intrinsic Pontine Glioma
Diffuse Intrinsic Pontine Glioma 		87 0 1 1.1E-02 0 0
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		94 48 1 1.1E-02 1 2.1E-02
CUI: C1849265
Disease: Overgrowth
Overgrowth 		103 0 1 9.7E-03 0 0
CUI: C1853237
Disease: Isolated cases
Isolated cases 		111 0 1 9.0E-03 0 0
CUI: C0149940
Disease: Sciatic Neuropathy
Sciatic Neuropathy 		115 0 1 8.7E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		135 0 1 7.4E-03 0 0
CUI: C4722099
Disease: High grade glioma
High grade glioma 		190 0 1 5.3E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 5.2E-03 0 0
CUI: C0013170
Disease: Drug habituation
Drug habituation 		196 0 1 5.1E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 1 4.7E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 0 1 3.8E-03 0 0