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: C0598589
Disease: Inherited neuropathies
Inherited neuropathies
104 0 23 9.7E-02 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 67 42 9.7E-02 2 2.7E-02
CUI: C0013421
Disease: Dystonia
Dystonia
453 0 53 9.5E-02 0 0
CUI: C0009676
Disease: Confusion
Confusion
75 0 20 9.5E-02 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus
213 0 32 9.5E-02 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia
133 0 25 9.5E-02 0 0
CUI: C0085660
Disease: Aseptic necrosis
Aseptic necrosis
41 0 17 9.5E-02 0 0
CUI: C3887513
Disease: Avascular necrosis
Avascular necrosis
41 0 17 9.5E-02 0 0
CUI: C4553018
Disease: Avascular Necrosis, CTCAE
Avascular Necrosis, CTCAE
41 0 17 9.5E-02 0 0
CUI: C0085582
Disease: Retrobulbar Neuritis
Retrobulbar Neuritis
18 0 15 9.5E-02 0 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
91 0 21 9.3E-02 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
190 0 29 9.2E-02 0 0
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome
239 0 33 9.1E-02 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar
156 0 26 9.1E-02 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular
86 0 20 9.0E-02 0 0
CUI: C4020965
Disease: Cardiac diverticulum
Cardiac diverticulum
14 0 14 9.0E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
389 0 45 9.0E-02 0 0
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic
75 37 19 9.0E-02 1 2.2E-02
CUI: C1262477
Disease: Weight decreased
Weight decreased
271 0 35 9.0E-02 0 0
CUI: C0237653
Disease: Immunologic hypersensitivity
Immunologic hypersensitivity
16 0 14 8.9E-02 0 0
CUI: C0022575
Disease: Keratoconjunctivitis Sicca
Keratoconjunctivitis Sicca
90 0 20 8.9E-02 0 0
CUI: C0001816
Disease: Agnosia
Agnosia
17 0 14 8.9E-02 0 0
CUI: C2732838
Disease: Neoplasm of skeletal system
Neoplasm of skeletal system
17 0 14 8.9E-02 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 68 83 8.8E-02 1 1.3E-02
Morphological abnormality of the pyramidal tract
18 0 14 8.8E-02 0 0