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: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.8E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.8E-03 0 0
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation 		226 0 1 2.9E-03 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		208 0 1 3.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.0E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 3.1E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 3.2E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 3.2E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 3.2E-03 0 0
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		183 0 1 3.3E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 3.3E-03 0 0
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		175 0 1 3.4E-03 0 0
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		173 0 1 3.4E-03 0 0
CUI: C0037763
Disease: Spasm
Spasm 		172 0 1 3.4E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 3.4E-03 0 0
CUI: C0008489
Disease: Chorea
Chorea 		168 0 1 3.5E-03 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		167 0 1 3.5E-03 0 0
CUI: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder) 		166 0 1 3.5E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 3.6E-03 0 0
CUI: C1285162
Disease: Degenerative disorder
Degenerative disorder 		160 0 1 3.6E-03 0 0
CUI: C4551720
Disease: Primary Ciliary Dyskinesia
Primary Ciliary Dyskinesia 		160 0 1 3.6E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 3.6E-03 0 0
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation 		157 0 1 3.6E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 3.6E-03 0 0
CUI: C2585653
Disease: Persistent atrial fibrillation
Persistent atrial fibrillation 		156 0 1 3.6E-03 0 0