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: C0338478
Disease: Idiopathic Myoclonic Epilepsy
Idiopathic Myoclonic Epilepsy
8 0 1 0.12 0 0
CUI: C0338479
Disease: Symptomatic Myoclonic Epilepsy
Symptomatic Myoclonic Epilepsy
8 0 1 0.12 0 0
CUI: C0393695
Disease: Early Childhood Epilepsy, Myoclonic
Early Childhood Epilepsy, Myoclonic
8 0 1 0.12 0 0
CUI: C0751120
Disease: Benign Infantile Myoclonic Epilepsy
Benign Infantile Myoclonic Epilepsy
8 0 1 0.12 0 0
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury
8 0 1 0.12 0 0
CUI: C1852289
Disease: Autoamputation of digits
Autoamputation of digits
8 0 1 0.12 0 0
CUI: C4732740
Disease: Acral ulceration
Acral ulceration
8 0 1 0.12 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2
9 0 1 0.11 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion
9 0 1 0.11 0 0
CUI: C0151827
Disease: Eye pain
Eye pain
10 0 1 1.0E-01 0 0
CUI: C0393703
Disease: Myoclonic Absence Epilepsy
Myoclonic Absence Epilepsy
10 0 1 1.0E-01 0 0
CUI: C1298685
Disease: Chronic pain syndrome
Chronic pain syndrome
10 0 1 1.0E-01 0 0
CUI: C4025676
Disease: Abnormality of the knee
Abnormality of the knee
10 0 1 1.0E-01 0 0
CUI: C0030578
Disease: Paronychia Inflammation
Paronychia Inflammation
11 0 1 9.1E-02 0 0
CUI: C0151854
Disease: Abnormal platelets
Abnormal platelets
11 0 1 9.1E-02 0 0
CUI: C0438414
Disease: Myoclonic Encephalopathy
Myoclonic Encephalopathy
11 0 1 9.1E-02 0 0
CUI: C0917800
Disease: Epilepsy, Myoclonic, Infantile
Epilepsy, Myoclonic, Infantile
11 0 1 9.1E-02 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension
11 0 1 9.1E-02 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion
12 0 1 8.3E-02 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures
12 0 1 8.3E-02 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status
12 0 1 8.3E-02 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple
13 0 1 7.7E-02 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER
13 0 1 7.7E-02 0 0
Generalized Epilepsy with Febrile Seizures Plus
13 0 1 7.7E-02 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity
14 0 1 7.1E-02 0 0