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 0 1 0.20 0 0
CUI: C1847627
Disease: Dyskinesia, Familial, with Facial Myokymia
Dyskinesia, Familial, with Facial Myokymia 		1 5 1 0.20 1 0.20
CUI: C1854369
Disease: Spinocerebellar ataxia 14
Spinocerebellar ataxia 14 		7 0 2 0.20 0 0
CUI: C3809327
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14 		1 0 1 0.20 0 0
CUI: C4022593
Disease: Tremor by anatomical site
Tremor by anatomical site 		1 0 1 0.20 0 0
CUI: C4310662
Disease: SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE 		1 0 1 0.20 0 0
CUI: C4706415
Disease: Spectrin-associated autosomal recessive cerebellar ataxia
Spectrin-associated autosomal recessive cerebellar ataxia 		1 0 1 0.20 0 0
CUI: C4707562
Disease: Autoimmune encephalopathy with parasomnia and obstructive sleep apnea
Autoimmune encephalopathy with parasomnia and obstructive sleep apnea 		2 0 1 0.17 0 0
CUI: C1112261
Disease: Gaze palsy
Gaze palsy 		3 0 1 0.14 0 0
CUI: C1859098
Disease: Chorea, Benign Familial
Chorea, Benign Familial 		3 0 1 0.14 0 0
CUI: C0268279
Disease: Lipofuscinosis
Lipofuscinosis 		4 0 1 0.12 0 0
CUI: C2242579
Disease: Lingual dystonia
Lingual dystonia 		4 0 1 0.12 0 0
CUI: C4510873
Disease: Atypical juvenile parkinsonism
Atypical juvenile parkinsonism 		4 0 1 0.12 0 0
CUI: C1142448
Disease: Apraxia of eyelid
Apraxia of eyelid 		5 0 1 0.11 0 0
CUI: C1834207
Disease: Ceroid Lipofuscinosis, Neuronal, Parry Type
Ceroid Lipofuscinosis, Neuronal, Parry Type 		5 0 1 0.11 0 0
CUI: C1853558
Disease: Jerky ocular pursuit movements
Jerky ocular pursuit movements 		5 0 1 0.11 0 0
CUI: C1858501
Disease: Spinocerebellar Ataxia 12
Spinocerebellar Ataxia 12 		5 0 1 0.11 0 0
CUI: C0270749
Disease: Marie Cerebellar Ataxia
Marie Cerebellar Ataxia 		6 0 1 1.0E-01 0 0
CUI: C1836149
Disease: Axial dystonia
Axial dystonia 		6 0 1 1.0E-01 0 0
CUI: C1849096
Disease: Infantile onset spinocerebellar ataxia
Infantile onset spinocerebellar ataxia 		6 0 1 1.0E-01 0 0
CUI: C4021898
Disease: Upper limb hypertonia
Upper limb hypertonia 		6 4 1 1.0E-01 1 0.25
CUI: C4025609
Disease: EMG: axonal abnormality
EMG: axonal abnormality 		6 0 1 1.0E-01 0 0
CUI: C4476759
Disease: Stooped posture
Stooped posture 		6 0 1 1.0E-01 0 0
CUI: C1835265
Disease: Lymphedema, microcephaly and chorioretinopathy syndrome
Lymphedema, microcephaly and chorioretinopathy syndrome 		7 0 1 9.1E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 3 9.1E-02 0 0