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: C0162671
Disease: MELAS Syndrome
MELAS Syndrome
80 53 29 0.28 9 0.16
Chronic progressive external ophthalmoplegia
50 0 18 0.22 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
59 0 19 0.21 0 0
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 22 0.15 0 0
Abnormality of mitochondrial metabolism
21 0 9 0.14 0 0
CUI: C0745730
Disease: Multiple lipomata
Multiple lipomata
38 0 11 0.14 0 0
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
Optic Atrophy, Hereditary, Leber
100 46 18 0.14 1 1.7E-02
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode
27 0 9 0.13 0 0
CUI: C0022541
Disease: Kearns-Sayre syndrome
Kearns-Sayre syndrome
29 0 9 0.13 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology
30 0 9 0.12 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia
41 0 10 0.12 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality
23 0 8 0.12 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis
61 0 12 0.12 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood
46 0 10 0.11 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures
105 0 16 0.11 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
31 0 8 0.11 0 0
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies
53 0 10 0.11 0 0
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting
43 0 9 0.11 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 21 0.11 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas
33 0 8 0.11 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 10 0.10 0 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness
35 0 8 0.10 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome
48 0 9 1.0E-01 0 0
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax
49 0 9 9.9E-02 0 0
CUI: C3151970
Disease: MERRF/MELAS OVERLAP SYNDROME
MERRF/MELAS OVERLAP SYNDROME
5 5 5 9.8E-02 2 0.12