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: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2
18 0 8 6.1E-02 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations
178 18 17 6.0E-02 1 1.0E-02
Primary Progressive Nonfluent Aphasia
21 0 8 5.9E-02 0 0
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
560 179 38 5.9E-02 2 7.8E-03
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease
186 0 17 5.8E-02 0 0
CUI: C4041080
Disease: Neurocognitive Disorders
Neurocognitive Disorders
79 0 11 5.8E-02 0 0
CUI: C0234133
Disease: Extrapyramidal sign
Extrapyramidal sign
116 0 13 5.8E-02 0 0
CUI: C0497327
Disease: Dementia
Dementia
816 176 51 5.7E-02 6 2.4E-02
CUI: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic
82 0 11 5.7E-02 0 0
CUI: C0016667
Disease: Fragile X Syndrome
Fragile X Syndrome
194 0 17 5.7E-02 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases
66 0 10 5.6E-02 0 0
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease
255 41 20 5.6E-02 4 3.4E-02
Disruptive, Impulse Control, and Conduct Disorders
67 9 10 5.6E-02 1 1.1E-02
CUI: C0871189
Disease: Psychotic symptom
Psychotic symptom
86 21 11 5.6E-02 1 1.0E-02
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
718 159 44 5.5E-02 6 2.6E-02
CUI: C1392786
Disease: Cognitive changes
Cognitive changes
50 15 9 5.5E-02 2 2.2E-02
CUI: C1096063
Disease: Drug Resistant Epilepsy
Drug Resistant Epilepsy
184 0 16 5.5E-02 0 0
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
320 215 23 5.5E-02 2 6.8E-03
Primary Progressive Aphasia (disorder)
51 11 9 5.5E-02 1 1.1E-02
CUI: C0392678
Disease: Swallowing problem
Swallowing problem
13 0 7 5.5E-02 0 0
CUI: C0031572
Disease: Phobia, Social
Phobia, Social
33 0 8 5.4E-02 0 0
CUI: C0233397
Disease: Psychological symptom
Psychological symptom
33 0 8 5.4E-02 0 0
CUI: C0242510
Disease: Drug usage
Drug usage
170 0 15 5.4E-02 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism
34 3 8 5.4E-02 1 1.2E-02
Behavioral variant of frontotemporal dementia
35 0 8 5.4E-02 0 0