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: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 1.00 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 1.00 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 1.00 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 1.00 0 0
CUI: C1839785
Disease: Folate-dependent fragile site at Xq28
Folate-dependent fragile site at Xq28 		1 0 1 1.00 0 0
CUI: C3275367
Disease: Impaired tandem gait
Impaired tandem gait 		1 0 1 1.00 0 0
CUI: C3275521
Disease: CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME
CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME 		1 0 1 1.00 0 0
CUI: C4024650
Disease: Congenital macroorchidism
Congenital macroorchidism 		1 0 1 1.00 0 0
CUI: C0476236
Disease: Developmental symptoms
Developmental symptoms 		2 0 1 0.50 0 0
CUI: C0748071
Disease: psychosocial impairment
psychosocial impairment 		2 0 1 0.50 0 0
CUI: C0949331
Disease: Gonadal Agenesis
Gonadal Agenesis 		2 0 1 0.50 0 0
CUI: C1839782
Disease: Macroorchidism, postpubertal
Macroorchidism, postpubertal 		2 0 1 0.50 0 0
CUI: C2678248
Disease: Mood instability
Mood instability 		2 0 1 0.50 0 0
CUI: C0236794
Disease: Panic disorder without agoraphobia
Panic disorder without agoraphobia 		3 0 1 0.33 0 0
CUI: C1364667
Disease: Adrenalitis
Adrenalitis 		3 0 1 0.33 0 0
CUI: C1842605
Disease: SCHIZOPHRENIA 11
SCHIZOPHRENIA 11 		3 0 1 0.33 0 0
CUI: C2930861
Disease: Premature ovarian failure, familial
Premature ovarian failure, familial 		3 0 1 0.33 0 0
CUI: C3809278
Disease: EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET 		3 0 1 0.33 0 0
CUI: C3825158
Disease: Learning disabled
Learning disabled 		3 0 1 0.33 0 0
CUI: C0004444
Disease: Avoidant Personality Disorder
Avoidant Personality Disorder 		4 0 1 0.25 0 0
CUI: C0236801
Disease: Phobia, Specific
Phobia, Specific 		4 0 1 0.25 0 0
CUI: C4022575
Disease: Inertia
Inertia 		4 0 1 0.25 0 0
CUI: C4324720
Disease: Autoimmune thyroid disorder
Autoimmune thyroid disorder 		4 0 1 0.25 0 0
CUI: C0012746
Disease: Dissociative disorder
Dissociative disorder 		6 0 1 0.17 0 0
CUI: C0042023
Disease: Increased frequency of micturition
Increased frequency of micturition 		6 0 1 0.17 0 0