Source: CURATED ×
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: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 0 1 0.14 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 0 1 0.14 0 0
CUI: C2749007
Disease: Chromosome Xq28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome 		1 0 1 0.14 0 0
CUI: C2751584
Disease: Neurodegeneration Due To Cerebral Folate Transport Deficiency
Neurodegeneration Due To Cerebral Folate Transport Deficiency 		1 0 1 0.14 0 0
CUI: C3151063
Disease: MACULAR DEGENERATION, AGE-RELATED, 5
MACULAR DEGENERATION, AGE-RELATED, 5 		1 0 1 0.14 0 0
CUI: C3203733
Disease: Precordial Catch Syndrome
Precordial Catch Syndrome 		1 0 1 0.14 0 0
CUI: C3551173
Disease: UV-SENSITIVE SYNDROME 1
UV-SENSITIVE SYNDROME 1 		1 0 1 0.14 0 0
CUI: C3713418
Disease: Ppm-X Syndrome
Ppm-X Syndrome 		1 0 1 0.14 0 0
CUI: C3714043
Disease: Trisomy Xq28
Trisomy Xq28 		1 0 1 0.14 0 0
CUI: C4310783
Disease: PREMATURE OVARIAN FAILURE 11
PREMATURE OVARIAN FAILURE 11 		1 0 1 0.14 0 0
CUI: C0035333
Disease: Retinitis
Retinitis 		2 0 1 0.12 0 0
CUI: C0154874
Disease: Neuroretinitis
Neuroretinitis 		2 0 1 0.12 0 0
CUI: C0751037
Disease: Cockayne Syndrome, Type III
Cockayne Syndrome, Type III 		2 0 1 0.12 0 0
CUI: C1846058
Disease: Lubs X-linked mental retardation syndrome
Lubs X-linked mental retardation syndrome 		2 0 1 0.12 0 0
CUI: C0005899
Disease: Body Rocking
Body Rocking 		3 0 1 0.11 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		3 0 1 0.11 0 0
CUI: C0009207
Disease: Cockayne Syndrome
Cockayne Syndrome 		3 0 1 0.11 0 0
CUI: C0018672
Disease: Head Banging
Head Banging 		3 0 1 0.11 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		3 0 1 0.11 0 0
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		3 0 1 0.11 0 0
CUI: C0751038
Disease: Cockayne Syndrome, Type II
Cockayne Syndrome, Type II 		3 0 1 0.11 0 0
CUI: C0751039
Disease: Cockayne Syndrome, Type I
Cockayne Syndrome, Type I 		3 0 1 0.11 0 0
CUI: C1833561
Disease: UV-Sensitive Syndrome
UV-Sensitive Syndrome 		3 0 1 0.11 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		4 0 1 1.0E-01 0 0
CUI: C0023380
Disease: Lethargy
Lethargy 		4 0 1 1.0E-01 0 0