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: C1867864
Disease: Poor fine motor coordination
Poor fine motor coordination
31 0 5 7.7E-02 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures
105 0 10 7.5E-02 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms
53 0 6 7.0E-02 0 0
CUI: C0338478
Disease: Idiopathic Myoclonic Epilepsy
Idiopathic Myoclonic Epilepsy
8 0 3 6.8E-02 0 0
CUI: C0338479
Disease: Symptomatic Myoclonic Epilepsy
Symptomatic Myoclonic Epilepsy
8 0 3 6.8E-02 0 0
CUI: C0393695
Disease: Early Childhood Epilepsy, Myoclonic
Early Childhood Epilepsy, Myoclonic
8 0 3 6.8E-02 0 0
CUI: C0751120
Disease: Benign Infantile Myoclonic Epilepsy
Benign Infantile Myoclonic Epilepsy
8 0 3 6.8E-02 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure
8 0 3 6.8E-02 0 0
Febrile infection related epilepsy syndrome
8 0 3 6.8E-02 0 0
CUI: C4049830
Disease: Focal seizures, afebril
Focal seizures, afebril
25 0 4 6.7E-02 0 0
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin
91 0 8 6.6E-02 0 0
CUI: C0393703
Disease: Myoclonic Absence Epilepsy
Myoclonic Absence Epilepsy
10 0 3 6.5E-02 0 0
CUI: C0438414
Disease: Myoclonic Encephalopathy
Myoclonic Encephalopathy
11 0 3 6.4E-02 0 0
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures
30 0 4 6.2E-02 0 0
CUI: C0019147
Disease: Hepatic Coma
Hepatic Coma
14 0 3 6.0E-02 0 0
Photosensitive tonic-clonic seizures
14 0 3 6.0E-02 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance
211 411 14 5.9E-02 4 9.3E-03
CUI: C0149958
Disease: Complex partial seizures
Complex partial seizures
140 0 10 5.9E-02 0 0
CUI: C0393702
Disease: Myoclonic Astatic Epilepsy
Myoclonic Astatic Epilepsy
16 0 3 5.8E-02 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn
17 0 3 5.7E-02 0 0
CUI: C4023499
Disease: Generalized clonic seizures
Generalized clonic seizures
18 0 3 5.6E-02 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy
19 0 3 5.5E-02 0 0
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior
19 0 3 5.5E-02 0 0
Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System
2 0 2 5.1E-02 0 0
DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES
2 17 2 5.1E-02 10 0.32