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: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79 		1 0 1 0.12 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 43 1 0.12 2 4.3E-02
CUI: C2129647
Disease: menstrual symptoms
menstrual symptoms 		1 0 1 0.12 0 0
CUI: C2677682
Disease: Rett Syndrome, Zappella Variant
Rett Syndrome, Zappella Variant 		1 0 1 0.12 0 0
CUI: C2749007
Disease: Chromosome Xq28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome 		1 0 1 0.12 0 0
CUI: C2749022
Disease: Chromosome Xp11.23-P11.22 Duplication Syndrome
Chromosome Xp11.23-P11.22 Duplication Syndrome 		1 0 1 0.12 0 0
CUI: C2931847
Disease: Type I familial incomplete male pseudohermaphroditism
Type I familial incomplete male pseudohermaphroditism 		1 0 1 0.12 0 0
CUI: C3276611
Disease: Absent or delayed speech development
Absent or delayed speech development 		1 0 1 0.12 0 0
CUI: C3279839
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 7
MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 		1 0 1 0.12 0 0
CUI: C3661485
Disease: 17p11.2 Monosomy
17p11.2 Monosomy 		1 0 1 0.12 0 0
CUI: C3713418
Disease: Ppm-X Syndrome
Ppm-X Syndrome 		1 0 1 0.12 0 0
CUI: C3714043
Disease: Trisomy Xq28
Trisomy Xq28 		1 0 1 0.12 0 0
CUI: C4021041
Disease: Maternal fever in pregnancy
Maternal fever in pregnancy 		1 0 1 0.12 0 0
CUI: C4021338
Disease: Broad proximal phalanx of the hallux
Broad proximal phalanx of the hallux 		1 1 1 0.12 1 0.20
CUI: C4022561
Disease: Maternal first trimester fever
Maternal first trimester fever 		1 0 1 0.12 0 0
CUI: C4022733
Disease: Widened cerebral subarachnoid space
Widened cerebral subarachnoid space 		1 0 1 0.12 0 0
CUI: C4022860
Disease: Maternal anticardiolipin antibody positive
Maternal anticardiolipin antibody positive 		1 0 1 0.12 0 0
CUI: C4023493
Disease: Beta-EEG
Beta-EEG 		1 1 1 0.12 1 0.20
CUI: C4023494
Disease: Alpha-EEG
Alpha-EEG 		1 1 1 0.12 1 0.20
CUI: C4025796
Disease: Abnormality of the fingertips
Abnormality of the fingertips 		1 1 1 0.12 1 0.20
CUI: C4225255
Disease: YUAN-HAREL-LUPSKI SYNDROME
YUAN-HAREL-LUPSKI SYNDROME 		1 0 1 0.12 0 0
CUI: C4225276
Disease: EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME
EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME 		1 19 1 0.12 1 4.3E-02
CUI: C4520847
Disease: Immunoglobulin G subclass deficiency (finding)
Immunoglobulin G subclass deficiency (finding) 		1 1 1 0.12 1 0.20
CUI: C4703574
Disease: Sleep-wake inversion
Sleep-wake inversion 		1 0 1 0.12 0 0
CUI: C4749281
Disease: Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation 		1 0 1 0.12 0 0