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 1.0E-01 0 0
CUI: C0455990
Disease: Immune Hydrops Fetalis
Immune Hydrops Fetalis 		1 0 1 1.0E-01 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 1.0E-01 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 1.0E-01 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 1.0E-01 0 0
CUI: C1839785
Disease: Folate-dependent fragile site at Xq28
Folate-dependent fragile site at Xq28 		1 0 1 1.0E-01 0 0
CUI: C1845285
Disease: Martin-Probst Deafness-Mental Retardation Syndrome
Martin-Probst Deafness-Mental Retardation Syndrome 		1 0 1 1.0E-01 0 0
CUI: C1855840
Disease: HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME
HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C1856129
Disease: Thyroid lymphangiectasia
Thyroid lymphangiectasia 		1 0 1 1.0E-01 0 0
CUI: C1856139
Disease: Pleural lymphangiectasia
Pleural lymphangiectasia 		1 0 1 1.0E-01 0 0
CUI: C1856471
Disease: Short metacarpals with rounded proximal ends
Short metacarpals with rounded proximal ends 		1 0 1 1.0E-01 0 0
CUI: C1861627
Disease: Butterfly vertebral arch
Butterfly vertebral arch 		1 0 1 1.0E-01 0 0
CUI: C1866053
Disease: Deafness, Congenital Heart Defects, and Posterior Embryotoxon
Deafness, Congenital Heart Defects, and Posterior Embryotoxon 		1 0 1 1.0E-01 0 0
CUI: C3264595
Disease: Agoraphobia without panic disorder
Agoraphobia without panic disorder 		1 0 1 1.0E-01 0 0
CUI: C3275367
Disease: Impaired tandem gait
Impaired tandem gait 		1 0 1 1.0E-01 0 0
CUI: C3275521
Disease: CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME
CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C3278147
Disease: GELEOPHYSIC DYSPLASIA 1
GELEOPHYSIC DYSPLASIA 1 		1 0 1 1.0E-01 0 0
CUI: C3554373
Disease: AUTISM, SUSCEPTIBILITY TO, 18
AUTISM, SUSCEPTIBILITY TO, 18 		1 0 1 1.0E-01 0 0
CUI: C4021132
Disease: Supraventricular tachycardia with an accessory connection mediated pathway
Supraventricular tachycardia with an accessory connection mediated pathway 		1 0 1 1.0E-01 0 0
CUI: C4023371
Disease: Proportionate tall stature
Proportionate tall stature 		1 0 1 1.0E-01 0 0
CUI: C4024650
Disease: Congenital macroorchidism
Congenital macroorchidism 		1 0 1 1.0E-01 0 0
CUI: C4085597
Disease: CHOPS SYNDROME
CHOPS SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C4303594
Disease: Deafness and intellectual disability Martin Probst type syndrome
Deafness and intellectual disability Martin Probst type syndrome 		1 0 1 1.0E-01 0 0
CUI: C4310667
Disease: ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY
ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY 		1 0 1 1.0E-01 0 0
CUI: C0344975
Disease: Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Intact Ventricular Septum 		2 0 1 9.1E-02 0 0