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 mitochondria in muscle tissue
39 0 1 2.6E-02 0 0
Abnormal morphology of the cerebellar cortex
2 0 1 0.50 0 0
Abnormal thalamic MRI signal intensity
4 0 1 0.25 0 0
Abnormality of the autonomic nervous system
3 0 1 0.33 0 0
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion
10 0 1 1.0E-01 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 5.0E-03 0 0
CUI: C1321756
Disease: Achalasia
Achalasia
40 0 1 2.5E-02 0 0
CUI: C0205710
Disease: Alpers Syndrome (disorder)
Alpers Syndrome (disorder)
28 0 1 3.6E-02 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea
37 2 1 2.7E-02 1 0.14
CUI: C0003467
Disease: Anxiety
Anxiety
1048 0 1 9.5E-04 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 1 1.2E-03 0 0
CUI: C3683791
Disease: Ataxia Neuropathy Spectrum
Ataxia Neuropathy Spectrum
2 0 1 0.50 0 0
CUI: C0240991
Disease: Ataxia, Sensory
Ataxia, Sensory
35 0 1 2.9E-02 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar
156 0 1 6.4E-03 0 0
CUI: C0234366
Disease: Ataxic
Ataxic
15 0 1 6.7E-02 0 0
CUI: C0004158
Disease: Athetosis
Athetosis
39 0 1 2.6E-02 0 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
939 0 1 1.1E-03 0 0
Atrophy/Degeneration affecting the brainstem
27 0 1 3.7E-02 0 0
Atrophy/Degeneration involving the spinal cord
2 0 1 0.50 0 0
CUI: C1852271
Disease: Auditory neuropathy
Auditory neuropathy
24 0 1 4.2E-02 0 0
Autosomal dominant cerebellar ataxia
31 0 1 3.2E-02 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy
59 0 1 1.7E-02 0 0
CUI: C1865916
Disease: Bilateral ptosis
Bilateral ptosis
50 0 1 2.0E-02 0 0
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
1183 0 1 8.5E-04 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.7E-03 0 0