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: C0339666
Disease: Nystagmus and other irregular eye movements
Nystagmus and other irregular eye movements 		1 1 1 1.00 1 0.33
CUI: C4706415
Disease: Spectrin-associated autosomal recessive cerebellar ataxia
Spectrin-associated autosomal recessive cerebellar ataxia 		1 0 1 1.00 0 0
CUI: C0270871
Disease: Facial Myokymia
Facial Myokymia 		5 0 1 0.20 0 0
CUI: C1853558
Disease: Jerky ocular pursuit movements
Jerky ocular pursuit movements 		5 0 1 0.20 0 0
CUI: C1849096
Disease: Infantile onset spinocerebellar ataxia
Infantile onset spinocerebellar ataxia 		6 0 1 0.17 0 0
CUI: C1835265
Disease: Lymphedema, microcephaly and chorioretinopathy syndrome
Lymphedema, microcephaly and chorioretinopathy syndrome 		7 0 1 0.14 0 0
CUI: C1854369
Disease: Spinocerebellar ataxia 14
Spinocerebellar ataxia 14 		7 0 1 0.14 0 0
CUI: C0852975
Disease: Congenital cerebellar ataxia
Congenital cerebellar ataxia 		8 0 1 0.12 0 0
CUI: C4551521
Disease: Kinetic tremor
Kinetic tremor 		13 5 1 7.7E-02 1 0.14
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		14 0 1 7.1E-02 0 0
CUI: C1839042
Disease: Upper motor neuron dysfunction
Upper motor neuron dysfunction 		16 0 1 6.2E-02 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades 		18 0 1 5.6E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 0 1 4.8E-02 0 0
CUI: C1853761
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 		21 0 1 4.8E-02 0 0
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement 		22 10 1 4.5E-02 1 8.3E-02
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 1 4.0E-02 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position 		26 0 1 3.8E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 1 3.2E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 1 3.0E-02 0 0
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4 		36 0 1 2.8E-02 0 0
CUI: C0234518
Disease: Slurred speech
Slurred speech 		39 0 1 2.6E-02 0 0
CUI: C0700636
Disease: Focal nodular hyperplasia of liver
Focal nodular hyperplasia of liver 		39 0 1 2.6E-02 0 0
CUI: C3179455
Disease: Niemann-Pick Disease, Type C1
Niemann-Pick Disease, Type C1 		43 0 1 2.3E-02 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 2.1E-02 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5 		48 0 1 2.1E-02 0 0