Source: BEFREE ×
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: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked 		128 0 24 0.18 0 0
CUI: C0796225
Disease: Mental Retardation, X-Linked 19
Mental Retardation, X-Linked 19 		5 0 4 0.15 0 0
CUI: C0265252
Disease: Coffin-Lowry syndrome
Coffin-Lowry syndrome 		23 0 6 0.14 0 0
CUI: C0220775
Disease: RUSSELL-SILVER SYNDROME, X-LINKED
RUSSELL-SILVER SYNDROME, X-LINKED 		4 0 3 0.11 0 0
CUI: C0796250
Disease: PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME
PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME 		4 0 3 0.11 0 0
CUI: C2720163
Disease: Placental Steroid Sulfatase Deficiency
Placental Steroid Sulfatase Deficiency 		17 0 4 0.10 0 0
CUI: C0265339
Disease: Borjeson-Forssman-Lehmann syndrome
Borjeson-Forssman-Lehmann syndrome 		9 0 3 9.4E-02 0 0
CUI: C0751157
Disease: FRAXE Syndrome
FRAXE Syndrome 		9 0 3 9.4E-02 0 0
CUI: C0743101
Disease: developmentally delayed
developmentally delayed 		11 0 3 8.8E-02 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		38 0 5 8.5E-02 0 0
CUI: C1306341
Disease: Mental handicap
Mental handicap 		26 0 4 8.3E-02 0 0
CUI: C0238210
Disease: Malrotation of kidney
Malrotation of kidney 		2 0 2 7.7E-02 0 0
CUI: C0796244
Disease: MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED (disorder)
MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED (disorder) 		2 0 2 7.7E-02 0 0
CUI: C1845499
Disease: MENTAL RETARDATION, X-LINKED 77
MENTAL RETARDATION, X-LINKED 77 		2 0 2 7.7E-02 0 0
CUI: C0796135
Disease: Renpenning syndrome 1
Renpenning syndrome 1 		19 0 3 7.1E-02 0 0
CUI: C0006009
Disease: Borderline intellectual disability
Borderline intellectual disability 		5 0 2 6.9E-02 0 0
CUI: C1720275
Disease: Gonadotropin releasing factor deficiency
Gonadotropin releasing factor deficiency 		5 0 2 6.9E-02 0 0
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		6 0 2 6.7E-02 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		38 0 4 6.7E-02 0 0
CUI: C0023882
Disease: Little's Disease
Little's Disease 		7 0 2 6.5E-02 0 0
CUI: C0175713
Disease: Aicardi's syndrome
Aicardi's syndrome 		7 0 2 6.5E-02 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		90 0 7 6.4E-02 0 0
CUI: C1845862
Disease: Creatine deficiency, X-linked
Creatine deficiency, X-linked 		9 0 2 6.1E-02 0 0
CUI: C0220766
Disease: Congenital hypoplasia of adrenal gland
Congenital hypoplasia of adrenal gland 		45 0 4 6.0E-02 0 0
CUI: C1864172
Disease: Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group G 		10 0 2 5.9E-02 0 0