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: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		1236 1451 27 2.0E-02 1 6.7E-04
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 579 6 5.6E-03 1 1.6E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment 		740 337 12 1.4E-02 4 1.1E-02
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		362 247 9 1.9E-02 1 3.4E-03
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		130 236 9 3.8E-02 1 3.6E-03
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		383 222 15 3.1E-02 3 1.1E-02
CUI: C0017601
Disease: Glaucoma
Glaucoma 		770 198 33 3.9E-02 1 4.1E-03
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 131 1 4.5E-03 1 5.7E-03
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 120 20 3.7E-02 1 6.1E-03
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 111 15 1.7E-02 2 1.3E-02
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases 		284 84 19 5.0E-02 4 3.2E-02
CUI: C0004134
Disease: Ataxia
Ataxia 		868 68 26 2.7E-02 1 8.9E-03
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		457 64 18 3.2E-02 1 9.3E-03
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma 		103 56 10 4.8E-02 2 2.0E-02
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 51 24 3.6E-02 4 4.3E-02
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
Optic Atrophy, Hereditary, Leber 		100 46 16 8.0E-02 1 1.1E-02
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		9 36 1 8.0E-03 1 1.3E-02
CUI: C3276549
Disease: OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY 		14 22 11 9.2E-02 9 0.16
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 21 5 2.4E-02 1 1.5E-02
CUI: C0023348
Disease: Leprosy, Lepromatous
Leprosy, Lepromatous 		94 17 2 9.6E-03 2 3.3E-02
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 17 1 5.4E-03 1 1.6E-02
CUI: C4551508
Disease: Dominant hereditary optic atrophy
Dominant hereditary optic atrophy 		16 14 16 0.14 14 0.31
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3 		12 13 6 4.9E-02 2 3.6E-02
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 12 5 1.5E-02 1 1.8E-02
CUI: C1833021
Disease: DEAFNESS, AUTOSOMAL DOMINANT 6
DEAFNESS, AUTOSOMAL DOMINANT 6 		1 11 1 8.5E-03 1 1.8E-02