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 0.12 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 0.12 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 0.12 0 0
CUI: C0855389
Disease: Renin decreased
Renin decreased 		1 0 1 0.12 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 0.12 0 0
CUI: C2676770
Disease: Birk-Barel Mental Retardation Dysmorphism Syndrome
Birk-Barel Mental Retardation Dysmorphism Syndrome 		1 0 1 0.12 0 0
CUI: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 		1 0 1 0.12 0 0
CUI: C2677793
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 6
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 6 		1 0 1 0.12 0 0
CUI: C2749872
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6 		1 0 1 0.12 0 0
CUI: C2750892
Disease: EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1
EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1 		1 0 1 0.12 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 0.12 0 0
CUI: C3553637
Disease: HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 		1 0 1 0.12 0 0
CUI: C4016713
Disease: EPISODIC ATAXIA, TYPE 2, AND EPILEPSY
EPISODIC ATAXIA, TYPE 2, AND EPILEPSY 		1 0 1 0.12 0 0
CUI: C4021571
Disease: Abnormal vestibulo-ocular reflex
Abnormal vestibulo-ocular reflex 		1 0 1 0.12 0 0
CUI: C4023088
Disease: EEG with generalized polyspikes
EEG with generalized polyspikes 		1 0 1 0.12 0 0
CUI: C4023544
Disease: Incisor macrodontia
Incisor macrodontia 		1 0 1 0.12 0 0
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		1 0 1 0.12 0 0
CUI: C4310716
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42 		1 0 1 0.12 0 0
CUI: C0238056
Disease: Chorea, Senile
Chorea, Senile 		2 0 1 0.11 0 0
CUI: C0477373
Disease: Other forms of migraine
Other forms of migraine 		2 0 1 0.11 0 0
CUI: C0699728
Disease: Chronic progressive chorea
Chronic progressive chorea 		2 0 1 0.11 0 0
CUI: C0856636
Disease: Transient hemiparesis
Transient hemiparesis 		2 0 1 0.11 0 0
CUI: C1735856
Disease: Migraine with Typical Aura
Migraine with Typical Aura 		2 0 1 0.11 0 0
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		2 0 1 0.11 0 0
CUI: C1846367
Disease: Spinocerebellar ataxia 19
Spinocerebellar ataxia 19 		2 0 1 0.11 0 0