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: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential 		55 0 21 0.23 0 0
CUI: C4021734
Disease: Abnormality of mitochondrial metabolism
Abnormality of mitochondrial metabolism 		21 0 14 0.22 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality 		23 0 14 0.21 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology 		30 0 15 0.21 0 0
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode 		27 0 14 0.20 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes 		31 0 14 0.19 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		33 0 14 0.18 0 0
CUI: C0009024
Disease: Clonus
Clonus 		60 0 18 0.18 0 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness 		35 0 14 0.18 0 0
CUI: C0745730
Disease: Multiple lipomata
Multiple lipomata 		38 0 14 0.17 0 0
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism 		48 0 15 0.16 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 14 0.16 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 11 0.16 0 0
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		43 0 14 0.16 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood 		46 0 14 0.16 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 0 20 0.15 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		48 0 14 0.15 0 0
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax 		49 0 14 0.15 0 0
CUI: C0018794
Disease: Heart Block
Heart Block 		58 0 15 0.15 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 15 0.15 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 1 11 0.15 1 0.20
CUI: C1843156
Disease: Progressive sensorineural hearing impairment
Progressive sensorineural hearing impairment 		78 28 17 0.14 1 3.1E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 0 13 0.14 0 0
CUI: C0020438
Disease: Hypercalciuria
Hypercalciuria 		60 0 14 0.13 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		95 14 18 0.13 1 5.6E-02