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: C1851959
Disease: Fluctuations in consciousness
Fluctuations in consciousness
10 0 5 0.22 0 0
CUI: C4021243
Disease: Abnormality of thalamus morphology
Abnormality of thalamus morphology
10 0 5 0.22 0 0
CUI: C4025706
Disease: Abnormal globus pallidus morphology
Abnormal globus pallidus morphology
10 0 5 0.22 0 0
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode
27 0 8 0.22 0 0
CUI: C1858427
Disease: Limited extraocular movements
Limited extraocular movements
11 0 5 0.21 0 0
CUI: C4025701
Disease: Abnormality of the cerebral cortex
Abnormality of the cerebral cortex
11 0 5 0.21 0 0
CUI: C1557375
Disease: Blurred Vision, CTCAE
Blurred Vision, CTCAE
26 0 7 0.19 0 0
CUI: C0020672
Disease: Hypothermia, natural
Hypothermia, natural
52 0 11 0.19 0 0
CUI: C1853141
Disease: Slow decrease in visual acuity
Slow decrease in visual acuity
27 0 7 0.18 0 0
Abnormality of mitochondrial metabolism
21 0 6 0.18 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate
87 0 16 0.18 0 0
CUI: C0344232
Disease: Blurred vision
Blurred vision
28 0 7 0.18 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis
61 0 12 0.18 0 0
CUI: C3805839
Disease: Central hypoventilation
Central hypoventilation
16 0 5 0.17 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality
23 0 6 0.17 0 0
CUI: C0234649
Disease: Abnormal saccadic eye movement
Abnormal saccadic eye movement
17 0 5 0.17 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
59 0 11 0.17 0 0
CUI: C4304725
Disease: Leber plus disease
Leber plus disease
4 0 3 0.16 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia
41 0 8 0.16 0 0
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology
21 0 5 0.15 0 0
CUI: C0745730
Disease: Multiple lipomata
Multiple lipomata
38 0 7 0.14 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology
30 0 6 0.14 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
31 0 6 0.14 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome
48 0 8 0.14 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 7 0.14 0 0