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: C0751919
Disease: Acquired Neuromyotonia
Acquired Neuromyotonia 		4 0 4 0.31 0 0
CUI: C3854373
Disease: Morvan syndrome
Morvan syndrome 		4 0 3 0.21 0 0
CUI: C0684219
Disease: Myokymia
Myokymia 		15 0 4 0.17 0 0
CUI: C2930824
Disease: Autoimmune limbic encephalitis
Autoimmune limbic encephalitis 		3 0 2 0.14 0 0
CUI: C4025704
Disease: Abnormality of the corticospinal tract
Abnormality of the corticospinal tract 		5 0 2 0.12 0 0
CUI: C4476591
Disease: Dysgenesis of the hippocampus
Dysgenesis of the hippocampus 		5 0 2 0.12 0 0
CUI: C1850765
Disease: Visual auras
Visual auras 		7 0 2 0.11 0 0
CUI: C0338430
Disease: Limbic Encephalitis
Limbic Encephalitis 		27 0 3 8.1E-02 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy 		14 0 2 8.0E-02 0 0
CUI: C0017570
Disease: Gingival Neoplasms
Gingival Neoplasms 		1 0 1 7.7E-02 0 0
CUI: C0029488
Disease: Other acute reactions to stress
Other acute reactions to stress 		1 0 1 7.7E-02 0 0
CUI: C0038131
Disease: Stammering
Stammering 		1 0 1 7.7E-02 0 0
CUI: C0234461
Disease: aphasic
aphasic 		1 0 1 7.7E-02 0 0
CUI: C0340776
Disease: Aneurysm of vein
Aneurysm of vein 		1 0 1 7.7E-02 0 0
CUI: C0343560
Disease: Congenital Varicella Syndrome
Congenital Varicella Syndrome 		1 0 1 7.7E-02 0 0
CUI: C0454542
Disease: Stuttering, Acquired
Stuttering, Acquired 		1 0 1 7.7E-02 0 0
CUI: C0454578
Disease: Receptive aphasia (finding)
Receptive aphasia (finding) 		1 0 1 7.7E-02 0 0
CUI: C0477972
Disease: Other specified congenital malformations of brain
Other specified congenital malformations of brain 		1 0 1 7.7E-02 0 0
CUI: C0497219
Disease: Hearing complaints (excluding H84-86)
Hearing complaints (excluding H84-86) 		1 0 1 7.7E-02 0 0
CUI: C0557875
Disease: Tired
Tired 		1 0 1 7.7E-02 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 7.7E-02 0 0
CUI: C0751527
Disease: Stuttering, Adult
Stuttering, Adult 		1 0 1 7.7E-02 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p 		1 0 1 7.7E-02 0 0
CUI: C1263892
Disease: Neoplasm of cauda equina
Neoplasm of cauda equina 		1 0 1 7.7E-02 0 0
CUI: C1527395
Disease: Ogilvie Syndrome
Ogilvie Syndrome 		1 0 1 7.7E-02 0 0