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: C0751157
Disease: FRAXE Syndrome
FRAXE Syndrome 		11 0 5 0.36 0 0
CUI: C1842605
Disease: SCHIZOPHRENIA 11
SCHIZOPHRENIA 11 		3 0 2 0.22 0 0
CUI: C2930861
Disease: Premature ovarian failure, familial
Premature ovarian failure, familial 		3 0 2 0.22 0 0
CUI: C3825158
Disease: Learning disabled
Learning disabled 		3 0 2 0.22 0 0
CUI: C0004444
Disease: Avoidant Personality Disorder
Avoidant Personality Disorder 		4 0 2 0.20 0 0
CUI: C1864172
Disease: Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group G 		10 0 3 0.20 0 0
CUI: C0743101
Disease: developmentally delayed
developmentally delayed 		11 0 3 0.19 0 0
CUI: C0233585
Disease: Foot tapping
Foot tapping 		1 0 1 0.12 0 0
CUI: C0342610
Disease: Hereditary cerebrovascular amyloidosis
Hereditary cerebrovascular amyloidosis 		1 0 1 0.12 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 0.12 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 0.12 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system 		1 0 1 0.12 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 0.12 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 0.12 0 0
CUI: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		1 0 1 0.12 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 0.12 0 0
CUI: C1839785
Disease: Folate-dependent fragile site at Xq28
Folate-dependent fragile site at Xq28 		1 0 1 0.12 0 0
CUI: C1856697
Disease: Mitochondrial malic enzyme reduced
Mitochondrial malic enzyme reduced 		1 0 1 0.12 0 0
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		1 0 1 0.12 0 0
CUI: C2751494
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT 		1 0 1 0.12 0 0
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		1 0 1 0.12 0 0
CUI: C3264595
Disease: Agoraphobia without panic disorder
Agoraphobia without panic disorder 		1 0 1 0.12 0 0
CUI: C3275367
Disease: Impaired tandem gait
Impaired tandem gait 		1 0 1 0.12 0 0
CUI: C3275521
Disease: CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME
CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME 		1 0 1 0.12 0 0
CUI: C3888307
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT 		1 0 1 0.12 0 0