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: C0338487
Disease: Benign paroxysmal vertigo of childhood
Benign paroxysmal vertigo of childhood 		0 1 0 0 1 7.1E-02
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 1.0E-01 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 1.0E-01 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 1.0E-01 0 0
CUI: C0338483
Disease: Migraine with Prolonged Aura
Migraine with Prolonged Aura 		1 0 1 1.0E-01 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 1.0E-01 0 0
CUI: C0477360
Disease: Other dystonia
Other dystonia 		1 0 1 1.0E-01 0 0
CUI: C0581882
Disease: Transient neurological symptoms
Transient neurological symptoms 		1 0 1 1.0E-01 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 1.0E-01 0 0
CUI: C1719382
Disease: Acquired torsion dystonia
Acquired torsion dystonia 		1 0 1 1.0E-01 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 1.0E-01 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 1 1 1.0E-01 1 7.1E-02
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 1.0E-01 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 1.0E-01 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 1.0E-01 0 0
CUI: C1865323
Disease: Migraine, Familial Basilar
Migraine, Familial Basilar 		1 0 1 1.0E-01 0 0
CUI: C2363747
Disease: Neurological decompensation
Neurological decompensation 		1 0 1 1.0E-01 0 0
CUI: C2674766
Disease: Myokymia 1
Myokymia 1 		1 0 1 1.0E-01 0 0
CUI: C2677106
Disease: Atrial Fibrillation, Familial, 7
Atrial Fibrillation, Familial, 7 		1 0 1 1.0E-01 0 0
CUI: C3149117
Disease: GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C3264000
Disease: Refractory juvenile myoclonic epilepsy
Refractory juvenile myoclonic epilepsy 		1 0 1 1.0E-01 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 1.0E-01 0 0
CUI: C3553788
Disease: ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 		1 38 1 1.0E-01 1 2.0E-02
CUI: C3553859
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 		1 0 1 1.0E-01 0 0
CUI: C3827273
Disease: Sudden Unexplained Death in Childhood
Sudden Unexplained Death in Childhood 		1 0 1 1.0E-01 0 0