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: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 0.12 0 0
CUI: C0752288
Disease: Adjustment Sleep Disorder
Adjustment Sleep Disorder 		1 0 1 0.12 0 0
CUI: C0752289
Disease: Environmental Sleep Disorder
Environmental Sleep Disorder 		1 0 1 0.12 0 0
CUI: C0752291
Disease: Limit-Setting Sleep Disorder
Limit-Setting Sleep Disorder 		1 0 1 0.12 0 0
CUI: C0752292
Disease: Nocturnal Eating-Drinking Syndrome
Nocturnal Eating-Drinking Syndrome 		1 0 1 0.12 0 0
CUI: C0752293
Disease: Sleep Disorders, Extrinsic
Sleep Disorders, Extrinsic 		1 0 1 0.12 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 0.12 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 0.12 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 0.12 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 8 1 0.12 1 8.3E-02
CUI: C1968537
Disease: Severe speech delay
Severe speech delay 		1 0 1 0.12 0 0
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 27 1 0.12 1 3.2E-02
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