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 2.4E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 2.4E-02 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 2.4E-02 0 0
CUI: C0265113
Disease: Progressing stroke
Progressing stroke 		1 0 1 2.4E-02 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty 		1 1 1 2.4E-02 1 0.50
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 2.4E-02 0 0
CUI: C0393725
Disease: Eating epilepsy
Eating epilepsy 		1 0 1 2.4E-02 0 0
CUI: C0751640
Disease: Cryptogenic Partial Complex Epilepsy
Cryptogenic Partial Complex Epilepsy 		1 0 1 2.4E-02 0 0
CUI: C0751641
Disease: Epilepsy, Symptomatic, Partial Complex
Epilepsy, Symptomatic, Partial Complex 		1 0 1 2.4E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 2.4E-02 0 0
CUI: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		1 0 1 2.4E-02 0 0
CUI: C1858674
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 		1 0 1 2.4E-02 0 0
CUI: C2675473
Disease: Mental Retardation, Autosomal Dominant 5
Mental Retardation, Autosomal Dominant 5 		1 0 1 2.4E-02 0 0
CUI: C2677326
Disease: Epileptic Encephalopathy, Early Infantile, 4
Epileptic Encephalopathy, Early Infantile, 4 		1 0 1 2.4E-02 0 0
CUI: C3151227
Disease: RETINITIS PIGMENTOSA 59
RETINITIS PIGMENTOSA 59 		1 0 1 2.4E-02 0 0
CUI: C3280415
Disease: COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA 		1 0 1 2.4E-02 0 0
CUI: C3280452
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12 		1 0 1 2.4E-02 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 2.4E-02 0 0
CUI: C3809624
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18 		1 0 1 2.4E-02 0 0
CUI: C3809824
Disease: PARKINSON DISEASE 20, EARLY-ONSET
PARKINSON DISEASE 20, EARLY-ONSET 		1 0 1 2.4E-02 0 0
CUI: C4014531
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24 		1 0 1 2.4E-02 0 0
CUI: C4015119
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26 		1 0 1 2.4E-02 0 0
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		1 0 1 2.4E-02 0 0
CUI: C4016713
Disease: EPISODIC ATAXIA, TYPE 2, AND EPILEPSY
EPISODIC ATAXIA, TYPE 2, AND EPILEPSY 		1 0 1 2.4E-02 0 0
CUI: C4021571
Disease: Abnormal vestibulo-ocular reflex
Abnormal vestibulo-ocular reflex 		1 0 1 2.4E-02 0 0