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: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 0 1 9.1E-02 0 0
CUI: C2677682
Disease: Rett Syndrome, Zappella Variant
Rett Syndrome, Zappella Variant 		1 0 1 9.1E-02 0 0
CUI: C2677903
Disease: Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia 		1 0 1 9.1E-02 0 0
CUI: C2678051
Disease: MENTAL RETARDATION, X-LINKED 94 (disorder)
MENTAL RETARDATION, X-LINKED 94 (disorder) 		1 0 1 9.1E-02 0 0
CUI: C2749007
Disease: Chromosome Xq28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome 		1 0 1 9.1E-02 0 0
CUI: C2750247
Disease: Polymicrogyria, Asymmetric
Polymicrogyria, Asymmetric 		1 0 1 9.1E-02 0 0
CUI: C2931317
Disease: Primary syphilis
Primary syphilis 		1 0 1 9.1E-02 0 0
CUI: C2931847
Disease: Type I familial incomplete male pseudohermaphroditism
Type I familial incomplete male pseudohermaphroditism 		1 0 1 9.1E-02 0 0
CUI: C3275438
Disease: AUTISM, SUSCEPTIBILITY TO, X-LINKED 5
AUTISM, SUSCEPTIBILITY TO, X-LINKED 5 		1 0 1 9.1E-02 0 0
CUI: C3713418
Disease: Ppm-X Syndrome
Ppm-X Syndrome 		1 0 1 9.1E-02 0 0
CUI: C3714043
Disease: Trisomy Xq28
Trisomy Xq28 		1 0 1 9.1E-02 0 0
CUI: C4022563
Disease: Abnormality of muscle size
Abnormality of muscle size 		1 0 1 9.1E-02 0 0
CUI: C4022860
Disease: Maternal anticardiolipin antibody positive
Maternal anticardiolipin antibody positive 		1 0 1 9.1E-02 0 0
CUI: C4024836
Disease: Generalized reticulate brown pigmentation
Generalized reticulate brown pigmentation 		1 0 1 9.1E-02 0 0
CUI: C4025796
Disease: Abnormality of the fingertips
Abnormality of the fingertips 		1 0 1 9.1E-02 0 0
CUI: C4305072
Disease: X-linked intellectual disability Van Esch type
X-linked intellectual disability Van Esch type 		1 0 1 9.1E-02 0 0
CUI: C4478383
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35
MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35 		1 0 1 9.1E-02 0 0
CUI: C4725675
Disease: Refractory Bladder Carcinoma
Refractory Bladder Carcinoma 		1 0 1 9.1E-02 0 0
CUI: C0233778
Disease: Synesthesia
Synesthesia 		2 0 1 8.3E-02 0 0
CUI: C0234523
Disease: Apraxia, Ideomotor
Apraxia, Ideomotor 		2 0 1 8.3E-02 0 0
CUI: C0265646
Disease: Talipes Calcaneovarus
Talipes Calcaneovarus 		2 0 1 8.3E-02 0 0
CUI: C0751355
Disease: Polymyoclonus
Polymyoclonus 		2 0 1 8.3E-02 0 0
CUI: C0796207
Disease: MENTAL RETARDATION, X-LINKED 2 (disorder)
MENTAL RETARDATION, X-LINKED 2 (disorder) 		2 0 1 8.3E-02 0 0
CUI: C0796220
Disease: MENTAL RETARDATION, X-LINKED 14
MENTAL RETARDATION, X-LINKED 14 		2 0 1 8.3E-02 0 0
CUI: C0796224
Disease: MENTAL RETARDATION, X-LINKED 18
MENTAL RETARDATION, X-LINKED 18 		2 0 1 8.3E-02 0 0