Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Neuronal loss in central nervous system
37 0 16 0.25 0 0
CUI: C0233522
Disease: Inappropriate behavior
Inappropriate behavior
14 0 11 0.24 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 12 0.22 0 0
Behavioral variant of frontotemporal dementia
35 0 14 0.22 0 0
CUI: C0240341
Disease: Micrographia
Micrographia
14 0 10 0.21 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis
14 0 10 0.21 0 0
CUI: C4021584
Disease: Frontotemporal cerebral atrophy
Frontotemporal cerebral atrophy
14 0 10 0.21 0 0
CUI: C0919974
Disease: Abulia
Abulia
9 0 9 0.21 0 0
Primary Progressive Nonfluent Aphasia
21 13 11 0.21 1 5.6E-02
CUI: C1838320
Disease: Hyperorality
Hyperorality
10 0 9 0.20 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity
10 0 9 0.20 0 0
CUI: C3805715
Disease: Short stepped shuffling gait
Short stepped shuffling gait
16 0 10 0.20 0 0
Abnormal lower motor neuron morphology
23 0 11 0.20 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior
13 0 9 0.19 0 0
CUI: C0241700
Disease: Voice Fatigue
Voice Fatigue
20 0 10 0.19 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 10 0.19 0 0
CUI: C0424290
Disease: Compulsive hoarding
Compulsive hoarding
14 0 9 0.19 0 0
CUI: C4072928
Disease: Spoken Word Recognition Deficit
Spoken Word Recognition Deficit
8 0 8 0.19 0 0
CUI: C0002018
Disease: Alexia
Alexia
9 0 8 0.18 0 0
CUI: C1839042
Disease: Upper motor neuron dysfunction
Upper motor neuron dysfunction
16 0 9 0.18 0 0
CUI: C4024956
Disease: Grammar-specific speech disorder
Grammar-specific speech disorder
10 0 8 0.18 0 0
CUI: C0003550
Disease: Broca Aphasia
Broca Aphasia
11 0 8 0.17 0 0
Abnormal brain FDG positron emission tomography
18 0 9 0.17 0 0
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation
26 0 10 0.17 0 0
CUI: C0085632
Disease: Apathy
Apathy
83 9 18 0.17 1 7.1E-02