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: C1857287
Disease: Stroke-like episode
Stroke-like episode
27 0 17 0.32 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
59 0 21 0.26 0 0
Abnormality of mitochondrial metabolism
21 0 13 0.25 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia
41 0 17 0.25 0 0
CUI: C2931092
Disease: Maternally Inherited Leigh Syndrome
Maternally Inherited Leigh Syndrome
12 0 11 0.25 0 0
Abnormality of Krebs cycle metabolism
12 0 11 0.25 0 0
CUI: C4022013
Disease: Multiple glomerular cysts
Multiple glomerular cysts
12 0 11 0.25 0 0
CUI: C4025585
Disease: Lacticaciduria
Lacticaciduria
12 0 11 0.25 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality
23 0 13 0.25 0 0
CUI: C1839532
Disease: Low plasma citrulline
Low plasma citrulline
14 0 11 0.24 0 0
CUI: C4531122
Disease: Abnormal speech prosody
Abnormal speech prosody
15 0 11 0.23 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome
48 0 17 0.23 0 0
CUI: C1842820
Disease: Cardiac conduction abnormality
Cardiac conduction abnormality
18 0 11 0.22 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology
30 0 13 0.22 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
31 0 13 0.21 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality
49 0 16 0.21 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis
61 0 18 0.21 0 0
CUI: C0745730
Disease: Multiple lipomata
Multiple lipomata
38 0 14 0.21 0 0
Segmental peripheral demyelination/remyelination
21 0 11 0.21 0 0
CUI: C1844945
Disease: Episodic respiratory distress
Episodic respiratory distress
21 0 11 0.21 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas
33 0 13 0.21 0 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness
35 0 13 0.20 0 0
CUI: C0271196
Disease: Scotoma, Centrocecal
Scotoma, Centrocecal
12 0 9 0.20 0 0
CUI: C0268630
Disease: Hyper-beta-alaninemia
Hyper-beta-alaninemia
33 0 12 0.19 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome
80 0 19 0.18 0 0