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: C0234259
Disease: Sensitive to smells
Sensitive to smells
1 0 1 9.1E-02 0 0
CUI: C0238637
Disease: Anal pain
Anal pain
1 0 1 9.1E-02 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain
1 0 1 9.1E-02 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia
1 0 1 9.1E-02 0 0
Rhabdomyomatous mesenchymal hamartoma
1 0 1 9.1E-02 0 0
Upper Extremity Deformities, Congenital
1 0 1 9.1E-02 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder
1 0 1 9.1E-02 0 0
CUI: C1274890
Disease: Midline cervical cleft
Midline cervical cleft
1 0 1 9.1E-02 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery
1 0 1 9.1E-02 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3
1 0 1 9.1E-02 0 0
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
1 0 1 9.1E-02 0 0
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
1 0 1 9.1E-02 0 0
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
1 0 1 9.1E-02 0 0
CUI: C2748541
Disease: Brugada Syndrome 5
Brugada Syndrome 5
1 0 1 9.1E-02 0 0
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10
1 0 1 9.1E-02 0 0
CUI: C2959380
Disease: Folliculosebaceous cystic hamartoma
Folliculosebaceous cystic hamartoma
1 0 1 9.1E-02 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11
1 0 1 9.1E-02 0 0
Refractory juvenile myoclonic epilepsy
1 0 1 9.1E-02 0 0
Early infantile epileptic encephalopathy, refractory
1 0 1 9.1E-02 0 0
CUI: C3809311
Disease: ATRIAL FIBRILLATION, FAMILIAL, 13
ATRIAL FIBRILLATION, FAMILIAL, 13
1 0 1 9.1E-02 0 0
Sudden Unexplained Death in Childhood
1 0 1 9.1E-02 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24
1 0 1 9.1E-02 0 0
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9
1 0 1 9.1E-02 0 0
CUI: C4020918
Disease: Dysharmonic bone age
Dysharmonic bone age
1 0 1 9.1E-02 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
1 0 1 9.1E-02 0 0