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: C0018099
Disease: Gout
Gout 		205 2354 4 1.4E-02 2 8.4E-04
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		2322 1085 30 1.3E-02 2 1.8E-03
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 579 29 2.8E-02 2 3.3E-03
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 411 5 1.7E-02 3 7.0E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		362 247 19 4.4E-02 2 7.5E-03
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		955 164 29 2.8E-02 3 1.6E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 144 16 0.13 1 6.1E-03
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		208 136 30 0.11 3 1.9E-02
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 135 25 2.7E-02 2 1.3E-02
CUI: C0011334
Disease: Dental caries
Dental caries 		330 126 8 1.9E-02 1 6.8E-03
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		508 121 12 2.0E-02 2 1.4E-02
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 120 38 7.7E-02 2 1.4E-02
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 111 35 4.2E-02 1 7.6E-03
CUI: C0442874
Disease: Neuropathy
Neuropathy 		484 110 41 7.6E-02 1 7.7E-03
CUI: C1834674
Disease: BETHLEM MYOPATHY 1
BETHLEM MYOPATHY 1 		17 108 1 9.2E-03 1 7.8E-03
CUI: C0028738
Disease: Nystagmus
Nystagmus 		833 95 44 5.0E-02 2 1.8E-02
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 93 15 6.8E-02 1 8.8E-03
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		557 91 6 9.3E-03 2 1.8E-02
CUI: C0038379
Disease: Strabismus
Strabismus 		716 89 15 1.9E-02 2 1.9E-02
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		536 87 39 6.6E-02 3 2.9E-02
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		19 84 3 2.8E-02 1 9.6E-03
CUI: C1836830
Disease: Developmental regression
Developmental regression 		333 80 23 5.7E-02 1 1.0E-02
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 77 4 3.9E-02 1 1.0E-02
CUI: C0018681
Disease: Headache
Headache 		338 75 6 1.4E-02 2 2.1E-02
CUI: C0004134
Disease: Ataxia
Ataxia 		868 68 52 5.7E-02 2 2.3E-02