Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Abnormal lower motor neuron morphology
23 0 12 0.39 0 0
Neuronal loss in the cerebral cortex
8 0 7 0.33 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 8 0.32 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 8 0.32 0 0
Degeneration of the lateral corticospinal tracts
21 0 9 0.28 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 8 0.26 0 0
CUI: C4025720
Disease: Pseudobulbar behavioral symptoms
Pseudobulbar behavioral symptoms
5 0 5 0.25 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 8 0.23 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 7 0.21 0 0
CUI: C0149632
Disease: Abnormality of the bladder
Abnormality of the bladder
9 0 5 0.21 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 6 0.18 0 0
CUI: C0270790
Disease: Quadriparesis
Quadriparesis
42 0 9 0.17 0 0
CUI: C0542223
Disease: Loss of speech
Loss of speech
37 0 8 0.16 0 0
CUI: C0221166
Disease: Paraparesis
Paraparesis
31 0 7 0.16 0 0
Fatigable weakness of swallowing muscles
39 0 8 0.16 0 0
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
25 0 6 0.15 0 0
Juvenile amyotrophic lateral sclerosis
20 0 5 0.14 0 0
Primary Progressive Nonfluent Aphasia
21 0 5 0.14 0 0
Amyotrophic Lateral Sclerosis With Dementia
30 0 6 0.14 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy
56 0 9 0.13 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm
48 0 8 0.13 0 0
CUI: C0233522
Disease: Inappropriate behavior
Inappropriate behavior
14 0 4 0.13 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy
48 0 8 0.13 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy
41 0 7 0.13 0 0
Complicated hereditary spastic paraplegia
16 0 4 0.12 0 0