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: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.1E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.2E-03 0 0
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders 		128 0 1 2.3E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 2.3E-03 0 0
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders 		121 0 1 2.4E-03 0 0
CUI: C0431380
Disease: Cortical Dysplasia
Cortical Dysplasia 		118 0 1 2.4E-03 0 0
CUI: C0029231
Disease: Organic Mental Disorders, Substance-Induced
Organic Mental Disorders, Substance-Induced 		115 0 1 2.4E-03 0 0
CUI: C4316881
Disease: Prescription Drug Abuse
Prescription Drug Abuse 		115 0 1 2.4E-03 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 0 1 2.4E-03 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 1 2.4E-03 0 0
CUI: C0600260
Disease: Lung Diseases, Obstructive
Lung Diseases, Obstructive 		104 0 1 2.5E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 2.5E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 2.5E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		94 0 1 2.5E-03 0 0
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		94 0 1 2.5E-03 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease 		92 0 1 2.5E-03 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		89 0 1 2.6E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 2.6E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 2.6E-03 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 1 2.6E-03 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology 		86 0 1 2.6E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 2.6E-03 0 0
CUI: C0236018
Disease: Aura
Aura 		83 0 1 2.6E-03 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 1 2.6E-03 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy 		83 0 1 2.6E-03 0 0