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 0.22 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 8 0.19 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 7 0.19 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 7 0.19 0 0
Degeneration of the lateral corticospinal tracts
21 0 8 0.18 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 8 0.17 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 7 0.16 0 0
Abnormal upper motor neuron morphology
20 0 7 0.16 0 0
CUI: C0270790
Disease: Quadriparesis
Quadriparesis
42 0 10 0.16 0 0
Abnormal lower motor neuron morphology
23 0 7 0.15 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy
41 6 8 0.12 1 1.0E-01
CUI: C0026884
Disease: Mutism
Mutism
47 0 8 0.11 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy
48 0 8 0.11 0 0
Fatigable weakness of swallowing muscles
39 0 7 0.11 0 0
Primary Progressive Nonfluent Aphasia
21 0 5 0.11 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition
56 0 8 0.10 0 0
Behavioral variant of frontotemporal dementia
35 0 6 1.0E-01 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm
48 0 7 9.7E-02 0 0
CUI: C1866772
Disease: Abnormal nerve conduction velocity
Abnormal nerve conduction velocity
5 0 3 9.1E-02 0 0
Amyotrophic Lateral Sclerosis With Dementia
30 0 5 8.9E-02 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia
56 0 7 8.7E-02 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy
56 0 7 8.7E-02 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 4 8.7E-02 0 0
CUI: C0085632
Disease: Apathy
Apathy
83 0 9 8.6E-02 0 0
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
8 0 3 8.3E-02 0 0