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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
5473 0 1 1.8E-04 0 0
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders
1515 0 1 6.6E-04 0 0
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
1296 0 1 7.7E-04 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1261 0 1 7.9E-04 0 0
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
977 0 1 1.0E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 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: C0002871
Disease: Anemia
Anemia
847 0 1 1.2E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 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: C1384666
Disease: hearing impairment
hearing impairment
740 0 1 1.3E-03 0 0
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
714 0 1 1.4E-03 0 0
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
592 0 1 1.7E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 1 1.7E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 1 1.8E-03 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
546 0 1 1.8E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.9E-03 0 0
CUI: C0040822
Disease: Tremor
Tremor
528 0 1 1.9E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 2.0E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE
477 0 1 2.1E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 0 1 2.1E-03 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
400 0 1 2.5E-03 0 0