Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Primary Progressive Nonfluent Aphasia
21 0 15 0.37 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
20 0 14 0.34 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 14 0.32 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 13 0.31 0 0
Abnormal lower motor neuron morphology
23 0 13 0.29 0 0
Primary Progressive Aphasia (disorder)
51 11 18 0.26 3 0.17
CUI: C0919974
Disease: Abulia
Abulia
9 0 9 0.26 0 0
CUI: C0233522
Disease: Inappropriate behavior
Inappropriate behavior
14 0 10 0.26 0 0
CUI: C0424290
Disease: Compulsive hoarding
Compulsive hoarding
14 0 10 0.26 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality
10 0 9 0.25 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity
10 0 9 0.25 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 9 0.23 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior
13 0 9 0.23 0 0
CUI: C0085632
Disease: Apathy
Apathy
83 0 22 0.23 0 0
CUI: C0003113
Disease: Anomia
Anomia
8 0 8 0.23 0 0
CUI: C4072928
Disease: Spoken Word Recognition Deficit
Spoken Word Recognition Deficit
8 0 8 0.23 0 0
CUI: C4021584
Disease: Frontotemporal cerebral atrophy
Frontotemporal cerebral atrophy
14 0 9 0.23 0 0
CUI: C0002018
Disease: Alexia
Alexia
9 0 8 0.22 0 0
CUI: C0240735
Disease: Personality Change
Personality Change
43 0 14 0.22 0 0
CUI: C4024956
Disease: Grammar-specific speech disorder
Grammar-specific speech disorder
10 0 8 0.22 0 0
CUI: C1839042
Disease: Upper motor neuron dysfunction
Upper motor neuron dysfunction
16 0 9 0.21 0 0
CUI: C0003550
Disease: Broca Aphasia
Broca Aphasia
11 0 8 0.21 0 0
Abnormal brain FDG positron emission tomography
18 0 9 0.20 0 0
CUI: C4024936
Disease: Temporal cortical atrophy
Temporal cortical atrophy
13 0 8 0.20 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition
56 0 15 0.20 0 0