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: C0240735
Disease: Personality Change
Personality Change
43 6 11 0.21 1 5.6E-02
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation
26 0 8 0.21 0 0
CUI: C0026884
Disease: Mutism
Mutism
47 0 11 0.19 0 0
Amyotrophic Lateral Sclerosis, Guam Form
36 0 9 0.19 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition
56 0 12 0.18 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia
18 0 6 0.18 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive
5 0 4 0.18 0 0
CUI: C3840049
Disease: Dysexecutive syndrome
Dysexecutive syndrome
5 0 4 0.18 0 0
Primary Progressive Aphasia (disorder)
51 0 11 0.18 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 6 0.18 0 0
Fatigable weakness of swallowing muscles
39 0 9 0.18 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 5 0.17 0 0
Neurofibrillary degeneration (morphologic abnormality)
21 0 6 0.17 0 0
Degeneration of the lateral corticospinal tracts
21 0 6 0.17 0 0
CUI: C0234144
Disease: Dysgraphia
Dysgraphia
43 0 9 0.16 0 0
CUI: C0542223
Disease: Loss of speech
Loss of speech
37 0 8 0.16 0 0
Neuronal loss in central nervous system
37 0 8 0.16 0 0
CUI: C3887640
Disease: Astrocytosis
Astrocytosis
37 0 8 0.16 0 0
CUI: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy
16 0 5 0.16 0 0
CUI: C0085632
Disease: Apathy
Apathy
83 9 14 0.16 1 4.8E-02
CUI: C0013528
Disease: Echolalia
Echolalia
39 0 8 0.15 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy
9 0 4 0.15 0 0
CUI: C0003635
Disease: Apraxias
Apraxias
71 0 12 0.15 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm
48 0 9 0.15 0 0
CUI: C0338457
Disease: Aphasia, Progressive
Aphasia, Progressive
10 0 4 0.15 0 0