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: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 1.00 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 1.00 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 0 1 1.00 0 0
CUI: C2931847
Disease: Type I familial incomplete male pseudohermaphroditism
Type I familial incomplete male pseudohermaphroditism 		1 0 1 1.00 0 0
CUI: C3713418
Disease: Ppm-X Syndrome
Ppm-X Syndrome 		1 0 1 1.00 0 0
CUI: C0233778
Disease: Synesthesia
Synesthesia 		2 0 1 0.50 0 0
CUI: C4024917
Disease: Congenital encephalopathy
Congenital encephalopathy 		3 0 1 0.33 0 0
CUI: C4707565
Disease: Bilateral polymicrogyria
Bilateral polymicrogyria 		3 0 1 0.33 0 0
CUI: C0220775
Disease: RUSSELL-SILVER SYNDROME, X-LINKED
RUSSELL-SILVER SYNDROME, X-LINKED 		4 0 1 0.25 0 0
CUI: C0340486
Disease: Induced ventricular tachycardia
Induced ventricular tachycardia 		4 0 1 0.25 0 0
CUI: C0796250
Disease: PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME
PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME 		4 0 1 0.25 0 0
CUI: C1096527
Disease: Mosaic trisomy 8 syndrome
Mosaic trisomy 8 syndrome 		4 0 1 0.25 0 0
CUI: C0342474
Disease: Lipoid congenital adrenal hyperplasia
Lipoid congenital adrenal hyperplasia 		5 0 1 0.20 0 0
CUI: C0796022
Disease: Lujan Fryns syndrome
Lujan Fryns syndrome 		5 0 1 0.20 0 0
CUI: C0948391
Disease: Convulsion in childhood
Convulsion in childhood 		5 0 1 0.20 0 0
CUI: C0795940
Disease: Filippi syndrome
Filippi syndrome 		6 0 1 0.17 0 0
CUI: C2678194
Disease: Mental Retardation, X-Linked, Syndromic, Christianson Type
Mental Retardation, X-Linked, Syndromic, Christianson Type 		6 0 1 0.17 0 0
CUI: C0023882
Disease: Little's Disease
Little's Disease 		7 0 1 0.14 0 0
CUI: C0175713
Disease: Aicardi's syndrome
Aicardi's syndrome 		7 0 1 0.14 0 0
CUI: C0231796
Disease: respiratory abnormalities
respiratory abnormalities 		7 0 1 0.14 0 0
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		7 0 1 0.14 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		7 0 1 0.14 0 0
CUI: C0349251
Disease: Behavioral syndrome associated with physiological disturbance and physical factors
Behavioral syndrome associated with physiological disturbance and physical factors 		8 0 1 0.12 0 0
CUI: C0750197
Disease: Sustained ventricular tachycardia
Sustained ventricular tachycardia 		9 0 1 0.11 0 0
CUI: C1970431
Disease: PITT-HOPKINS SYNDROME
PITT-HOPKINS SYNDROME 		9 0 1 0.11 0 0