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: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		135 0 9 5.2E-02 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 0 4 5.2E-02 0 0
CUI: C2675021
Disease: Narrow palpebral fissure
Narrow palpebral fissure 		34 0 4 5.2E-02 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 11 5.2E-02 0 0
CUI: C0240341
Disease: Micrographia
Micrographia 		14 0 3 5.2E-02 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		14 7 3 5.2E-02 3 0.15
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 3 5.2E-02 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 0 8 5.1E-02 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 246 10 5.1E-02 6 2.3E-02
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness 		57 0 5 5.1E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 39 8 5.0E-02 4 7.8E-02
CUI: C3553450
Disease: Profound global developmental delay
Profound global developmental delay 		58 20 5 5.0E-02 2 5.9E-02
CUI: C0263401
Disease: Cutis marmorata
Cutis marmorata 		80 9 6 5.0E-02 2 8.7E-02
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 11 5.0E-02 0 0
CUI: C4551560
Disease: Truncal obesity
Truncal obesity 		38 0 4 4.9E-02 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		60 12 5 4.9E-02 2 7.7E-02
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait 		18 0 3 4.8E-02 0 0
CUI: C2712334
Disease: Actual Aspiration
Actual Aspiration 		18 8 3 4.8E-02 2 9.1E-02
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 26 11 4.8E-02 2 5.0E-02
CUI: C0700201
Disease: Dyssomnias
Dyssomnias 		236 0 13 4.8E-02 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 5 4.8E-02 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		106 0 7 4.8E-02 0 0
CUI: C0037763
Disease: Spasm
Spasm 		172 9 10 4.8E-02 1 4.2E-02
CUI: C0079352
Disease: Congenital torticollis
Congenital torticollis 		19 6 3 4.8E-02 2 1.0E-01
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		19 7 3 4.8E-02 2 9.5E-02