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: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
3397 0 1 2.9E-04 0 0
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
2723 0 1 3.7E-04 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 3 3.5E-03 0 0
CUI: C0006111
Disease: Brain Diseases
Brain Diseases
345 0 1 2.9E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
441 0 1 2.3E-03 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
45 0 1 2.1E-02 0 0
Diabetes Mellitus, Non-Insulin-Dependent
3134 0 1 3.2E-04 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy
1215 0 1 8.2E-04 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy
89 0 1 1.1E-02 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
400 0 3 7.5E-03 0 0
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease
143 0 1 6.9E-03 0 0
CUI: C0022107
Disease: Irritable Mood
Irritable Mood
142 0 1 6.9E-03 0 0
Late-Infantile Neuronal Ceroid Lipfuscinosis
19 0 3 0.16 0 0
Adult Neuronal Ceroid Lipofuscinosis
16 0 3 0.19 0 0
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
3111 0 1 3.2E-04 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
505 0 1 2.0E-03 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
362 0 1 2.7E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 0 1 1.0E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 0 3 1.1E-02 0 0
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration
165 0 1 6.0E-03 0 0
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
977 0 1 1.0E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 1 1.8E-03 0 0
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
560 0 1 1.8E-03 0 0
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration
125 0 1 7.9E-03 0 0
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
714 0 1 1.4E-03 0 0