Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0270790
Disease: Quadriparesis
Quadriparesis
42 0 6 9.1E-02 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness
126 0 13 9.1E-02 0 0
CUI: C1456865
Disease: Ureteral Calculi
Ureteral Calculi
6 0 3 9.1E-02 0 0
Abnormal brain FDG positron emission tomography
18 0 4 9.1E-02 0 0
CUI: C0221166
Disease: Paraparesis
Paraparesis
31 0 5 8.9E-02 0 0
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
31 0 5 8.9E-02 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
20 0 4 8.7E-02 0 0
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
8 0 3 8.6E-02 0 0
Amyotrophic Lateral Sclerosis, Sporadic
173 0 16 8.6E-02 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease
186 0 17 8.5E-02 0 0
CUI: C0026884
Disease: Mutism
Mutism
47 0 6 8.5E-02 0 0
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration
165 0 15 8.3E-02 0 0
CUI: C0919974
Disease: Abulia
Abulia
9 0 3 8.3E-02 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy
48 0 6 8.3E-02 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality
10 0 3 8.1E-02 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity
10 0 3 8.1E-02 0 0
CUI: C3887640
Disease: Astrocytosis
Astrocytosis
37 0 5 8.1E-02 0 0
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
25 0 4 7.8E-02 0 0
CUI: C0205858
Disease: General Paralysis
General Paralysis
12 0 3 7.7E-02 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy
41 0 5 7.6E-02 0 0
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
27 0 4 7.5E-02 0 0
CUI: C0271148
Disease: Secondary Open Angle Glaucoma
Secondary Open Angle Glaucoma
13 0 3 7.5E-02 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition
56 0 6 7.5E-02 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior
13 0 3 7.5E-02 0 0
CUI: C0037763
Disease: Spasm
Spasm
172 0 14 7.4E-02 0 0