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: C0393698
Disease: Cryptogenic Infantile Spasms
Cryptogenic Infantile Spasms
6 0 6 0.25 0 0
CUI: C0393699
Disease: Symptomatic Infantile Spasms
Symptomatic Infantile Spasms
6 0 6 0.25 0 0
CUI: C0546878
Disease: Nodding spasm
Nodding spasm
6 0 6 0.25 0 0
CUI: C0553558
Disease: Jackknife Seizures
Jackknife Seizures
6 0 6 0.25 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia
6 0 6 0.25 0 0
CUI: C1527306
Disease: spasmus nutans
spasmus nutans
6 0 6 0.25 0 0
CUI: C1527366
Disease: Salaam Seizures
Salaam Seizures
6 0 6 0.25 0 0
Early infantile epileptic encephalopathy with suppression bursts
16 0 5 0.14 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy
13 0 3 8.8E-02 0 0
CUI: C1854465
Disease: TUBEROUS SCLEROSIS 1 (disorder)
TUBEROUS SCLEROSIS 1 (disorder)
2 0 2 8.3E-02 0 0
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic
82 0 8 8.2E-02 0 0
CUI: C0236018
Disease: Aura
Aura
82 0 8 8.2E-02 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy
82 0 8 8.2E-02 0 0
CUI: C0041341
Disease: Tuberous Sclerosis
Tuberous Sclerosis
3 0 2 8.0E-02 0 0
Fibrous skin tumor of tuberous sclerosis
3 0 2 8.0E-02 0 0
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR
3 0 2 8.0E-02 0 0
Focal Cortical Dysplasia of Taylor, Type IIa
3 0 2 8.0E-02 0 0
Focal Cortical Dysplasia of Taylor, Type IIb
3 0 2 8.0E-02 0 0
CUI: C0751674
Disease: Lymphangioleiomyomatosis
Lymphangioleiomyomatosis
5 0 2 7.4E-02 0 0
CUI: C2748910
Disease: Rett Syndrome, Atypical
Rett Syndrome, Atypical
5 0 2 7.4E-02 0 0
CUI: C0010481
Disease: Cushing Syndrome
Cushing Syndrome
6 0 2 7.1E-02 0 0
CUI: C0013415
Disease: Dysthymic Disorder
Dysthymic Disorder
6 0 2 7.1E-02 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
6 0 2 7.1E-02 0 0
CUI: C0338478
Disease: Idiopathic Myoclonic Epilepsy
Idiopathic Myoclonic Epilepsy
8 0 2 6.7E-02 0 0
CUI: C0338479
Disease: Symptomatic Myoclonic Epilepsy
Symptomatic Myoclonic Epilepsy
8 0 2 6.7E-02 0 0