Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
31 54 26 0.81 51 0.73
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
164 139 27 0.16 53 0.35
Amyotrophic Lateral Sclerosis, Sporadic
173 90 27 0.16 51 0.48
Amyotrophic Lateral Sclerosis With Dementia
30 0 4 7.5E-02 0 0
Amyotrophic Lateral Sclerosis, Guam Form
36 0 4 6.8E-02 0 0
Fatigable weakness of swallowing muscles
39 0 4 6.5E-02 0 0
Neuronal loss in the cerebral cortex
8 0 2 6.1E-02 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm
48 0 4 5.6E-02 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 2 5.3E-02 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 2 5.3E-02 0 0
Behavioral variant of frontotemporal dementia
35 0 3 5.1E-02 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia
56 0 4 5.1E-02 0 0
Fatigable weakness of respiratory muscles
60 0 4 4.8E-02 0 0
CUI: C0854193
Disease: Cognitive deterioration
Cognitive deterioration
39 0 3 4.8E-02 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia
18 0 2 4.7E-02 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 2 4.5E-02 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 2 4.5E-02 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
20 0 2 4.4E-02 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 2 4.4E-02 0 0
Abnormal upper motor neuron morphology
20 0 2 4.4E-02 0 0
CUI: C0522224
Disease: Paralysed
Paralysed
68 0 4 4.4E-02 0 0
Primary Progressive Nonfluent Aphasia
21 0 2 4.3E-02 0 0
Degeneration of the lateral corticospinal tracts
21 0 2 4.3E-02 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 2 4.2E-02 0 0
Abnormal lower motor neuron morphology
23 0 2 4.2E-02 0 0