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: C4225245
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14 		1 0 1 1.00 0 0
CUI: C4225257
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34 		1 0 1 1.00 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures 		5 0 1 0.20 0 0
CUI: C4518639
Disease: Epilepsy of infancy with migrating focal seizures
Epilepsy of infancy with migrating focal seizures 		7 0 1 0.14 0 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		8 0 1 0.12 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn 		17 0 1 5.9E-02 0 0
CUI: C4021758
Disease: Delayed CNS myelination
Delayed CNS myelination 		21 0 1 4.8E-02 0 0
CUI: C0014558
Disease: Uncinate Epilepsy
Uncinate Epilepsy 		23 0 1 4.3E-02 0 0
CUI: C0393672
Disease: Epilepsy, Benign Psychomotor, Childhood
Epilepsy, Benign Psychomotor, Childhood 		23 0 1 4.3E-02 0 0
CUI: C0877017
Disease: Generalized tonic-clonic seizures with focal onset
Generalized tonic-clonic seizures with focal onset 		23 0 1 4.3E-02 0 0
CUI: C0342418
Disease: Hypothalamic hamartomas
Hypothalamic hamartomas 		29 0 1 3.4E-02 0 0
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal 		29 0 1 3.4E-02 0 0
CUI: C0037036
Disease: Sialorrhea
Sialorrhea 		32 0 1 3.1E-02 0 0
CUI: C2938983
Disease: Focal cortical dysplasia
Focal cortical dysplasia 		44 0 1 2.3E-02 0 0
CUI: C0023186
Disease: Learning Disorders
Learning Disorders 		46 0 1 2.2E-02 0 0
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes 		46 0 1 2.2E-02 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		57 0 1 1.8E-02 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 1.6E-02 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy 		63 0 1 1.6E-02 0 0
CUI: C0393734
Disease: Complex Partial Status Epilepticus
Complex Partial Status Epilepticus 		68 0 1 1.5E-02 0 0
CUI: C0751524
Disease: Simple Partial Status Epilepticus
Simple Partial Status Epilepticus 		68 0 1 1.5E-02 0 0
CUI: C0751522
Disease: Status Epilepticus, Subclinical
Status Epilepticus, Subclinical 		69 0 1 1.4E-02 0 0
CUI: C0751523
Disease: Non-Convulsive Status Epilepticus
Non-Convulsive Status Epilepticus 		71 0 1 1.4E-02 0 0
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy 		74 0 1 1.4E-02 0 0
CUI: C0010633
Disease: Cystadenoma
Cystadenoma 		75 0 1 1.3E-02 0 0