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: C1857308
Disease: Anterior cortical cataract
Anterior cortical cataract 		1 0 1 1.00 0 0
CUI: C4021468
Disease: Deviation of the 2nd finger
Deviation of the 2nd finger 		1 0 1 1.00 0 0
CUI: C4023650
Disease: Posterior cortical cataract
Posterior cortical cataract 		1 0 1 1.00 0 0
CUI: C1840088
Disease: Limited wrist movement
Limited wrist movement 		3 0 1 0.33 0 0
CUI: C0029125
Disease: Optic Atrophies, Hereditary
Optic Atrophies, Hereditary 		4 0 1 0.25 0 0
CUI: C1855126
Disease: 3-Methylglutaconic Aciduria Type IV
3-Methylglutaconic Aciduria Type IV 		4 0 1 0.25 0 0
CUI: C4040739
Disease: 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome 		4 0 1 0.25 0 0
CUI: C0344523
Disease: Cataract, congenital, cerulean type 1
Cataract, congenital, cerulean type 1 		6 0 1 0.17 0 0
CUI: C1112768
Disease: Anterior subcapsular cataract
Anterior subcapsular cataract 		10 0 1 1.0E-01 0 0
CUI: C1852470
Disease: Extrapyramidal muscular rigidity
Extrapyramidal muscular rigidity 		11 0 1 9.1E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3 		12 13 1 8.3E-02 3 0.21
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 0 1 7.1E-02 0 0
CUI: C0240914
Disease: Romberg's sign positive
Romberg's sign positive 		15 0 1 6.7E-02 0 0
CUI: C4551508
Disease: Dominant hereditary optic atrophy
Dominant hereditary optic atrophy 		16 0 1 6.2E-02 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria 		20 0 1 5.0E-02 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 1 4.8E-02 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		24 0 1 4.2E-02 0 0
CUI: C0155017
Disease: Color Blindness, Blue
Color Blindness, Blue 		25 0 1 4.0E-02 0 0
CUI: C1867103
Disease: Limited elbow extension
Limited elbow extension 		26 0 1 3.8E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2 		30 0 1 3.3E-02 0 0
CUI: C0558845
Disease: Reflex, Ankle, Absent
Reflex, Ankle, Absent 		33 0 1 3.0E-02 0 0
CUI: C0751093
Disease: Dystonia, Limb
Dystonia, Limb 		42 0 1 2.4E-02 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 1 2.3E-02 0 0
CUI: C3887709
Disease: Optic Neuropathy
Optic Neuropathy 		54 0 1 1.9E-02 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 0 1 1.8E-02 0 0