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 4.3E-02 0 0
CUI: C0238637
Disease: Anal pain
Anal pain
1 0 1 4.3E-02 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain
1 0 1 4.3E-02 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia
1 0 1 4.3E-02 0 0
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum
1 0 1 4.3E-02 0 0
Rhabdomyomatous mesenchymal hamartoma
1 0 1 4.3E-02 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome
1 0 1 4.3E-02 0 0
CUI: C1274890
Disease: Midline cervical cleft
Midline cervical cleft
1 0 1 4.3E-02 0 0
Continuous Muscle Fiber Activity, Hereditary
1 0 1 4.3E-02 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3
1 0 1 4.3E-02 0 0
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
1 0 1 4.3E-02 0 0
CUI: C1846171
Disease: Lissencephaly, X-Linked, 2
Lissencephaly, X-Linked, 2
1 0 1 4.3E-02 0 0
Hydranencephaly and Abnormal Genitalia
1 0 1 4.3E-02 0 0
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
1 0 1 4.3E-02 0 0
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
1 0 1 4.3E-02 0 0
CUI: C2674766
Disease: Myokymia 1
Myokymia 1
1 0 1 4.3E-02 0 0
Epileptic Encephalopathy, Early Infantile, 4
1 0 1 4.3E-02 0 0
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
1 0 1 4.3E-02 0 0
CUI: C2748541
Disease: Brugada Syndrome 5
Brugada Syndrome 5
1 0 1 4.3E-02 0 0
CUI: C2750247
Disease: Polymicrogyria, Asymmetric
Polymicrogyria, Asymmetric
1 0 1 4.3E-02 0 0
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10
1 0 1 4.3E-02 0 0
CUI: C2959380
Disease: Folliculosebaceous cystic hamartoma
Folliculosebaceous cystic hamartoma
1 0 1 4.3E-02 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11
1 0 1 4.3E-02 0 0
Refractory juvenile myoclonic epilepsy
1 0 1 4.3E-02 0 0
Early infantile epileptic encephalopathy, refractory
1 0 1 4.3E-02 0 0