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: C0393524
Disease: Cerebellar Ataxia, Late Onset
Cerebellar Ataxia, Late Onset
9 0 1 0.11 0 0
CUI: C0012619
Disease: disc disorder
disc disorder
13 0 1 7.7E-02 0 0
CUI: C0038017
Disease: Congenital spondylolisthesis
Congenital spondylolisthesis
17 0 1 5.9E-02 0 0
CUI: C0036396
Disease: Sciatica
Sciatica
24 0 1 4.2E-02 0 0
CUI: C0038016
Disease: Spondylolisthesis
Spondylolisthesis
28 0 1 3.6E-02 0 0
CUI: C0742028
Disease: Cerebellar vermis atrophy
Cerebellar vermis atrophy
32 0 1 3.1E-02 0 0
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4
36 0 1 2.8E-02 0 0
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia
36 0 1 2.8E-02 0 0
Fenestration (morphologic abnormality)
43 0 1 2.3E-02 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5
48 0 1 2.1E-02 0 0
CUI: C0221775
Disease: Lumbar disc disease
Lumbar disc disease
49 0 1 2.0E-02 0 0
Degeneration of lumbar intervertebral disc
50 0 1 2.0E-02 0 0
CUI: C3714534
Disease: dowling-degos disease
dowling-degos disease
53 0 1 1.9E-02 0 0
CUI: C1843921
Disease: Postural instability
Postural instability
60 0 1 1.7E-02 0 0
Hypertrophic disorder of skin, unspecified
62 0 1 1.6E-02 0 0
Spinocerebellar Ataxia Type 6 (disorder)
64 0 1 1.6E-02 0 0
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition
72 0 1 1.4E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
76 0 1 1.3E-02 0 0
CUI: C0024713
Disease: Manic Disorder
Manic Disorder
76 0 1 1.3E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2
76 0 1 1.3E-02 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7
78 0 1 1.3E-02 0 0
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities
83 0 1 1.2E-02 0 0
CUI: C0011119
Disease: Decompression Sickness
Decompression Sickness
98 0 1 1.0E-02 0 0
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1
102 0 1 9.8E-03 0 0
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome
104 0 1 9.6E-03 0 0