Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Abnormality of mitochondrial metabolism
21 0 14 0.38 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality
23 0 14 0.36 0 0
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode
27 0 14 0.33 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
31 0 14 0.30 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia
41 0 16 0.29 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas
33 0 14 0.29 0 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness
35 0 14 0.27 0 0
CUI: C0745730
Disease: Multiple lipomata
Multiple lipomata
38 0 14 0.26 0 0
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism
48 0 15 0.24 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood
46 0 14 0.23 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome
48 0 14 0.22 0 0
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting
43 0 13 0.22 0 0
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax
49 0 14 0.22 0 0
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity
58 0 15 0.21 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 15 0.20 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 14 0.20 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality
49 0 13 0.20 0 0
CUI: C0018794
Disease: Heart Block
Heart Block
58 0 14 0.19 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
59 0 14 0.19 0 0
CUI: C0020438
Disease: Hypercalciuria
Hypercalciuria
60 0 14 0.18 0 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction
87 0 18 0.18 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis
61 0 14 0.18 0 0
CUI: C0424448
Disease: Mask-like facies
Mask-like facies
64 0 14 0.17 0 0
CUI: C0271196
Disease: Scotoma, Centrocecal
Scotoma, Centrocecal
12 0 6 0.17 0 0
CUI: C2931092
Disease: Maternally Inherited Leigh Syndrome
Maternally Inherited Leigh Syndrome
12 0 6 0.17 0 0