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: C0750931
Disease: Arnold-Chiari Malformation, Type III
Arnold-Chiari Malformation, Type III 		1 0 1 9.1E-02 0 0
CUI: C0750932
Disease: Arnold-Chiari Malformation, Type IV
Arnold-Chiari Malformation, Type IV 		1 0 1 9.1E-02 0 0
CUI: C0751527
Disease: Stuttering, Adult
Stuttering, Adult 		1 0 1 9.1E-02 0 0
CUI: C0751528
Disease: Stuttering, Childhood
Stuttering, Childhood 		1 0 1 9.1E-02 0 0
CUI: C0751529
Disease: Stuttering, Developmental
Stuttering, Developmental 		1 0 1 9.1E-02 0 0
CUI: C1266177
Disease: Dysembryoplastic neuroepithelial tumor
Dysembryoplastic neuroepithelial tumor 		1 0 1 9.1E-02 0 0
CUI: C1266181
Disease: Dysplastic gangliocytoma of cerebellum (Lhermitte-Duclos)
Dysplastic gangliocytoma of cerebellum (Lhermitte-Duclos) 		1 0 1 9.1E-02 0 0
CUI: C1835047
Disease: MELANOMA, CUTANEOUS MALIGNANT, 1
MELANOMA, CUTANEOUS MALIGNANT, 1 		1 0 1 9.1E-02 0 0
CUI: C1860050
Disease: Cloverleaf skull
Cloverleaf skull 		1 0 1 9.1E-02 0 0
CUI: C1959620
Disease: Dihydropyrimidine Dehydrogenase Deficiency
Dihydropyrimidine Dehydrogenase Deficiency 		1 0 1 9.1E-02 0 0
CUI: C2750246
Disease: Pitt-Hopkins-Like Syndrome 1
Pitt-Hopkins-Like Syndrome 1 		1 0 1 9.1E-02 0 0
CUI: C2751642
Disease: GLIOMA SUSCEPTIBILITY 2
GLIOMA SUSCEPTIBILITY 2 		1 0 1 9.1E-02 0 0
CUI: C3151380
Disease: SCHIZOPHRENIA 15
SCHIZOPHRENIA 15 		1 0 1 9.1E-02 0 0
CUI: C3280479
Disease: PITT-HOPKINS-LIKE SYNDROME 2
PITT-HOPKINS-LIKE SYNDROME 2 		1 0 1 9.1E-02 0 0
CUI: C3806402
Disease: EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION 		1 0 1 9.1E-02 0 0
CUI: C3806917
Disease: CRANIOSYNOSTOSIS 4
CRANIOSYNOSTOSIS 4 		1 0 1 9.1E-02 0 0
CUI: C3808494
Disease: CHROMOSOME 2p16.3 DELETION SYNDROME
CHROMOSOME 2p16.3 DELETION SYNDROME 		1 0 1 9.1E-02 0 0
CUI: C3839609
Disease: Complex craniosynostosis
Complex craniosynostosis 		1 0 1 9.1E-02 0 0
CUI: C4015141
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 29
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 		1 0 1 9.1E-02 0 0
CUI: C4225350
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32 		1 0 1 9.1E-02 0 0
CUI: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome 		1 0 1 9.1E-02 0 0
CUI: C4310679
Disease: CHITAYAT SYNDROME
CHITAYAT SYNDROME 		1 0 1 9.1E-02 0 0
CUI: C4310833
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN 		1 0 1 9.1E-02 0 0
CUI: C4552043
Disease: Cortical dysplasia with focal epilepsy syndrome
Cortical dysplasia with focal epilepsy syndrome 		1 0 1 9.1E-02 0 0
CUI: C4707866
Disease: Familial lambdoid synostosis
Familial lambdoid synostosis 		1 0 1 9.1E-02 0 0