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: C2751829
Disease: Ventricular Fibrillation, Paroxysmal Familial, 2
Ventricular Fibrillation, Paroxysmal Familial, 2 		1 0 1 0.50 0 0
CUI: C3501946
Disease: Microcephaly with Chorioretinopathy, Autosomal Dominant
Microcephaly with Chorioretinopathy, Autosomal Dominant 		1 0 1 0.50 0 0
CUI: C4225375
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 		1 0 1 0.50 0 0
CUI: C1142305
Disease: Melanonychia
Melanonychia 		2 0 1 0.33 0 0
CUI: C4017668
Disease: VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO 		2 0 1 0.33 0 0
CUI: C0152205
Disease: Alternating esotropia
Alternating esotropia 		3 0 1 0.25 0 0
CUI: C2363771
Disease: Myopic astigmatism
Myopic astigmatism 		4 0 1 0.20 0 0
CUI: C0002938
Disease: Aneuploidy
Aneuploidy 		5 0 1 0.17 0 0
CUI: C0229197
Disease: Retinal fold (finding)
Retinal fold (finding) 		5 0 1 0.17 0 0
CUI: C0521683
Disease: Chorioretinal degeneration
Chorioretinal degeneration 		5 0 1 0.17 0 0
CUI: C4072867
Disease: obsolete Peripheral retinopathy
obsolete Peripheral retinopathy 		5 0 1 0.17 0 0
CUI: C1835265
Disease: Lymphedema, microcephaly and chorioretinopathy syndrome
Lymphedema, microcephaly and chorioretinopathy syndrome 		7 0 1 0.12 0 0
CUI: C3150852
Disease: EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION 		7 0 1 0.12 0 0
CUI: C0543891
Disease: Neuroleptic-Induced Tardive Dyskinesia
Neuroleptic-Induced Tardive Dyskinesia 		8 0 1 0.11 0 0
CUI: C1257806
Disease: Chromosomal Instability
Chromosomal Instability 		8 0 1 0.11 0 0
CUI: C0240182
Disease: Leukonychia
Leukonychia 		9 0 1 1.0E-01 0 0
CUI: C0339383
Disease: Choroidal and/or chorioretinal disorder
Choroidal and/or chorioretinal disorder 		9 0 1 1.0E-01 0 0
CUI: C0014733
Disease: Erysipelas
Erysipelas 		17 0 1 5.6E-02 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		18 0 1 5.3E-02 0 0
CUI: C0339539
Disease: Familial Exudative Vitreoretinopathy
Familial Exudative Vitreoretinopathy 		19 0 1 5.0E-02 0 0
CUI: C2931783
Disease: Amelogenesis imperfecta nephrocalcinosis
Amelogenesis imperfecta nephrocalcinosis 		19 0 1 5.0E-02 0 0
CUI: C0237849
Disease: Peeling of skin
Peeling of skin 		21 0 1 4.5E-02 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 1 4.5E-02 0 0
CUI: C0008733
Disease: Chylothorax
Chylothorax 		23 0 1 4.2E-02 0 0
CUI: C4025835
Disease: Abnormal nasolacrimal system morphology
Abnormal nasolacrimal system morphology 		23 0 1 4.2E-02 0 0