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: C0027651
Disease: Neoplasms
Neoplasms
10161 0 1 9.8E-05 0 0
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
3865 0 1 2.6E-04 0 0
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
2078 0 1 4.8E-04 0 0
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
1630 0 1 6.1E-04 0 0
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
977 0 1 1.0E-03 0 0
CUI: C0086543
Disease: Cataract
Cataract
878 0 1 1.1E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 1 1.2E-03 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
850 0 1 1.2E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 1 1.2E-03 0 0
CUI: C0497327
Disease: Dementia
Dementia
816 0 1 1.2E-03 0 0
Sensorineural Hearing Loss (disorder)
783 0 1 1.3E-03 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 1 1.3E-03 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 1 1.3E-03 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma
770 0 1 1.3E-03 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 0 1 1.3E-03 0 0
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
656 0 1 1.5E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 1 1.7E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 1 1.7E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.9E-03 0 0
CUI: C0021364
Disease: Male infertility
Male infertility
516 0 1 1.9E-03 0 0
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
978 0 2 2.0E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 2.0E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
454 0 1 2.2E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
441 0 1 2.3E-03 0 0
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
852 0 2 2.3E-03 0 0