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: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 3.8E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 3.8E-02 0 0
CUI: C0159104
Disease: Electrooculogram abnormal
Electrooculogram abnormal 		1 0 1 3.8E-02 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis 		1 0 1 3.8E-02 0 0
CUI: C0339666
Disease: Nystagmus and other irregular eye movements
Nystagmus and other irregular eye movements 		1 0 1 3.8E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 3.8E-02 0 0
CUI: C0451669
Disease: Neuropathy in association with hereditary ataxia
Neuropathy in association with hereditary ataxia 		1 0 1 3.8E-02 0 0
CUI: C0751668
Disease: Machado-Joseph Disease Type I
Machado-Joseph Disease Type I 		1 0 1 3.8E-02 0 0
CUI: C0751669
Disease: Machado-Joseph Disease Type II
Machado-Joseph Disease Type II 		1 0 1 3.8E-02 0 0
CUI: C0751670
Disease: Machado-Joseph Disease Type III
Machado-Joseph Disease Type III 		1 0 1 3.8E-02 0 0
CUI: C0751671
Disease: Machado-Joseph Disease Type IV
Machado-Joseph Disease Type IV 		1 0 1 3.8E-02 0 0
CUI: C1333422
Disease: epithelioid cell intraocular melanoma
epithelioid cell intraocular melanoma 		1 0 1 3.8E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 3.8E-02 0 0
CUI: C1836383
Disease: SPINOCEREBELLAR ATAXIA 27
SPINOCEREBELLAR ATAXIA 27 		1 0 1 3.8E-02 0 0
CUI: C1839565
Disease: Optic Atrophy Spastic Paraplegia Syndrome
Optic Atrophy Spastic Paraplegia Syndrome 		1 0 1 3.8E-02 0 0
CUI: C1862359
Disease: Facial-lingual fasciculations
Facial-lingual fasciculations 		1 0 1 3.8E-02 0 0
CUI: C1865416
Disease: Pallor of dorsal columns of the spinal cord
Pallor of dorsal columns of the spinal cord 		1 0 1 3.8E-02 0 0
CUI: C1865864
Disease: AMYOTROPHIC LATERAL SCLEROSIS 5
AMYOTROPHIC LATERAL SCLEROSIS 5 		1 0 1 3.8E-02 0 0
CUI: C1866039
Disease: EPISODIC ATAXIA, TYPE 5
EPISODIC ATAXIA, TYPE 5 		1 0 1 3.8E-02 0 0
CUI: C2675211
Disease: EPISODIC ATAXIA, TYPE 6 (disorder)
EPISODIC ATAXIA, TYPE 6 (disorder) 		1 0 1 3.8E-02 0 0
CUI: C2750887
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9 		1 0 1 3.8E-02 0 0
CUI: C2750888
Disease: EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6 		1 0 1 3.8E-02 0 0
CUI: C2931821
Disease: Nakamura Osame syndrome
Nakamura Osame syndrome 		1 0 1 3.8E-02 0 0
CUI: C3149907
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 		1 0 1 3.8E-02 0 0
CUI: C3280452
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12 		1 0 1 3.8E-02 0 0