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 the cerebral cortex
8 0 7 0.50 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 7 0.37 0 0
Abnormal lower motor neuron morphology
23 0 9 0.33 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 8 0.32 0 0
Abnormal upper motor neuron morphology
20 0 8 0.32 0 0
Primary Progressive Nonfluent Aphasia
21 0 8 0.31 0 0
Degeneration of the lateral corticospinal tracts
21 0 8 0.31 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 8 0.29 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 7 0.28 0 0
Fatigable weakness of swallowing muscles
39 0 10 0.24 0 0
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
8 0 4 0.24 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 6 0.23 0 0
Behavioral variant of frontotemporal dementia
35 0 9 0.23 0 0
Amyotrophic Lateral Sclerosis With Dementia
30 0 8 0.23 0 0
CUI: C0919974
Disease: Abulia
Abulia
9 0 4 0.22 0 0
CUI: C0349390
Disease: Non-fluent aphasia
Non-fluent aphasia
4 0 3 0.21 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality
10 0 4 0.21 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity
10 0 4 0.21 0 0
CUI: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy
16 0 5 0.21 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive
5 0 3 0.20 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm
48 0 10 0.20 0 0
Amyotrophic Lateral Sclerosis, Guam Form
36 0 8 0.20 0 0
CUI: C0221166
Disease: Paraparesis
Paraparesis
31 0 7 0.19 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
44 0 9 0.19 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior
13 0 4 0.18 0 0