Source: ALL
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: C1843156
Disease: Progressive sensorineural hearing impairment
Progressive sensorineural hearing impairment 		78 28 34 0.21 2 3.6E-02
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 46 0.20 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 23 0.17 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		33 0 18 0.14 0 0
CUI: C0011053
Disease: Deafness
Deafness 		62 0 21 0.13 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		72 0 21 0.12 0 0
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode 		27 0 16 0.12 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		48 0 18 0.12 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 19 0.12 0 0
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity 		58 0 18 0.11 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality 		49 0 17 0.11 0 0
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		43 0 16 0.11 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential 		55 0 17 0.11 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations 		178 0 29 0.11 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology 		30 0 14 0.11 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		80 0 18 0.10 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		61 0 16 9.9E-02 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 111 79 9.6E-02 1 7.1E-03
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		271 0 34 9.6E-02 0 0
CUI: C4021734
Disease: Abnormality of mitochondrial metabolism
Abnormality of mitochondrial metabolism 		21 0 12 9.5E-02 0 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis 		91 0 18 9.5E-02 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 20 9.4E-02 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality 		23 0 12 9.4E-02 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0 		108 0 19 9.2E-02 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0 		109 0 19 9.2E-02 0 0