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 4.0E-02 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 4.0E-02 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 4.0E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 4.0E-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 4.0E-02 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 4.0E-02 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts 		1 0 1 4.0E-02 0 0
CUI: C0339666
Disease: Nystagmus and other irregular eye movements
Nystagmus and other irregular eye movements 		1 0 1 4.0E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 4.0E-02 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia 		1 0 1 4.0E-02 0 0
CUI: C0810006
Disease: Acute cerebrovascular disease
Acute cerebrovascular disease 		1 0 1 4.0E-02 0 0
CUI: C0917967
Disease: Pupillary Functions, Abnormal
Pupillary Functions, Abnormal 		1 0 1 4.0E-02 0 0
CUI: C1257960
Disease: Mannosidase Deficiency Diseases
Mannosidase Deficiency Diseases 		1 0 1 4.0E-02 0 0
CUI: C1531646
Disease: Central topographic island
Central topographic island 		1 0 1 4.0E-02 0 0
CUI: C1608971
Disease: Optic nerve pallor
Optic nerve pallor 		1 0 1 4.0E-02 0 0
CUI: C1832471
Disease: Renal dysplasia diffuse cystic
Renal dysplasia diffuse cystic 		1 0 1 4.0E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 4.0E-02 0 0
CUI: C1836383
Disease: SPINOCEREBELLAR ATAXIA 27
SPINOCEREBELLAR ATAXIA 27 		1 0 1 4.0E-02 0 0
CUI: C1842577
Disease: JOUBERT SYNDROME 2
JOUBERT SYNDROME 2 		1 0 1 4.0E-02 0 0
CUI: C1847650
Disease: SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES 		1 0 1 4.0E-02 0 0
CUI: C1847725
Disease: SPINOCEREBELLAR ATAXIA 15
SPINOCEREBELLAR ATAXIA 15 		1 0 1 4.0E-02 0 0
CUI: C1849151
Disease: Hypermyelinated retinal nerve fibers
Hypermyelinated retinal nerve fibers 		1 0 1 4.0E-02 0 0
CUI: C1849152
Disease: Swan neck-like deformities of the fingers
Swan neck-like deformities of the fingers 		1 0 1 4.0E-02 0 0
CUI: C1851481
Disease: Erythrokeratodermia with ataxia
Erythrokeratodermia with ataxia 		1 0 1 4.0E-02 0 0
CUI: C1856974
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder) 		1 0 1 4.0E-02 0 0