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: C0026884
Disease: Mutism
Mutism 		47 0 1 2.1E-02 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 1 2.1E-02 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		51 0 1 2.0E-02 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 1.9E-02 0 0
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve 		59 0 1 1.7E-02 0 0
CUI: C0279612
Disease: Childhood Embryonal Rhabdomyosarcoma
Childhood Embryonal Rhabdomyosarcoma 		67 0 1 1.5E-02 0 0
CUI: C0683322
Disease: Mental impairment
Mental impairment 		67 0 1 1.5E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 1 1.5E-02 0 0
CUI: C0393734
Disease: Complex Partial Status Epilepticus
Complex Partial Status Epilepticus 		68 0 1 1.5E-02 0 0
CUI: C0751524
Disease: Simple Partial Status Epilepticus
Simple Partial Status Epilepticus 		68 0 1 1.5E-02 0 0
CUI: C0751522
Disease: Status Epilepticus, Subclinical
Status Epilepticus, Subclinical 		69 0 1 1.4E-02 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		71 0 1 1.4E-02 0 0
CUI: C0751523
Disease: Non-Convulsive Status Epilepticus
Non-Convulsive Status Epilepticus 		71 0 1 1.4E-02 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 1.4E-02 0 0
CUI: C0311335
Disease: Grand Mal Status Epilepticus
Grand Mal Status Epilepticus 		75 0 1 1.3E-02 0 0
CUI: C4288891
Disease: Infant T Acute Lymphoblastic Leukemia
Infant T Acute Lymphoblastic Leukemia 		75 0 1 1.3E-02 0 0
CUI: C0041207
Disease: Truncus Arteriosus, Persistent
Truncus Arteriosus, Persistent 		76 0 1 1.3E-02 0 0
CUI: C0270823
Disease: Petit mal status
Petit mal status 		78 0 1 1.3E-02 0 0
CUI: C3887506
Disease: Hyperkinesia
Hyperkinesia 		80 0 1 1.3E-02 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		81 0 1 1.2E-02 0 0
CUI: C0349788
Disease: Arrhythmogenic Right Ventricular Dysplasia
Arrhythmogenic Right Ventricular Dysplasia 		82 0 1 1.2E-02 0 0
CUI: C0236018
Disease: Aura
Aura 		83 0 1 1.2E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 1 1.2E-02 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy 		83 0 1 1.2E-02 0 0
CUI: C0497552
Disease: Congenital neurologic anomalies
Congenital neurologic anomalies 		84 0 1 1.2E-02 0 0