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: C0009398
Disease: Color vision defect
Color vision defect 		0 4 0 0 1 2.8E-02
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood 		0 20 0 0 1 1.9E-02
CUI: C0239377
Disease: Arm Pain
Arm Pain 		0 6 0 0 1 2.6E-02
CUI: C0278139
Disease: Moderate pain
Moderate pain 		0 1 0 0 1 3.0E-02
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 3.0E-02
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 2.9E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon 		0 1 0 0 1 3.0E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 2.4E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 3.0E-02
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia 		0 4 0 0 1 2.8E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.0E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		401 4389 1 2.1E-03 2 4.5E-04
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		399 0 1 2.1E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 1 2.2E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		338 0 1 2.4E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 1 2.5E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		319 0 1 2.5E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 1 2.6E-03 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 0 1 2.6E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 2 2.8E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		955 0 3 2.9E-03 0 0
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		560 0 2 3.2E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		234 0 1 3.2E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 3.3E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal 		227 0 1 3.3E-03 0 0