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: C0001889
Disease: Akinetic Mutism
Akinetic Mutism 		1 0 1 3.3E-02 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 3.3E-02 0 0
CUI: C0155379
Disease: Nystagmus associated with disorder of the vestibular system
Nystagmus associated with disorder of the vestibular system 		1 0 1 3.3E-02 0 0
CUI: C0242036
Disease: Paraplegia, Ataxic
Paraplegia, Ataxic 		1 0 1 3.3E-02 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 3.3E-02 0 0
CUI: C0278114
Disease: Paraplegia, Cerebral
Paraplegia, Cerebral 		1 0 1 3.3E-02 0 0
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal 		1 0 1 3.3E-02 0 0
CUI: C0280214
Disease: stage, nasopharyngeal cancer
stage, nasopharyngeal cancer 		1 0 1 3.3E-02 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts 		1 0 1 3.3E-02 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 3.3E-02 0 0
CUI: C0422879
Disease: CNS symptom
CNS symptom 		1 0 1 3.3E-02 0 0
CUI: C0451669
Disease: Neuropathy in association with hereditary ataxia
Neuropathy in association with hereditary ataxia 		1 0 1 3.3E-02 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid 		1 0 1 3.3E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 1 1 3.3E-02 1 1.00
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect 		1 0 1 3.3E-02 0 0
CUI: C0796036
Disease: Marinesco-Sjogren-like syndrome (MSLS)
Marinesco-Sjogren-like syndrome (MSLS) 		1 0 1 3.3E-02 0 0
CUI: C0796205
Disease: SPINOCEREBELLAR ATAXIA, X-LINKED 1
SPINOCEREBELLAR ATAXIA, X-LINKED 1 		1 0 1 3.3E-02 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait 		1 0 1 3.3E-02 0 0
CUI: C0917967
Disease: Pupillary Functions, Abnormal
Pupillary Functions, Abnormal 		1 0 1 3.3E-02 0 0
CUI: C1333422
Disease: epithelioid cell intraocular melanoma
epithelioid cell intraocular melanoma 		1 0 1 3.3E-02 0 0
CUI: C1832669
Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		1 0 1 3.3E-02 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia 		1 0 1 3.3E-02 0 0
CUI: C1837781
Disease: Increased subcutaneous truncal adipose tissue
Increased subcutaneous truncal adipose tissue 		1 0 1 3.3E-02 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex 		1 0 1 3.3E-02 0 0
CUI: C1844865
Disease: CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder) 		1 0 1 3.3E-02 0 0