Source: ALL
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: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors 		1 0 1 2.9E-02 0 0
CUI: C0220690
Disease: Macrocephaly, benign familial
Macrocephaly, benign familial 		1 0 1 2.9E-02 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 2.9E-02 0 0
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum 		1 0 1 2.9E-02 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome 		1 0 1 2.9E-02 0 0
CUI: C1456582
Disease: Vision Impairment and Blindness
Vision Impairment and Blindness 		1 0 1 2.9E-02 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 2.9E-02 0 0
CUI: C1720180
Disease: Confluent drusen
Confluent drusen 		1 0 1 2.9E-02 0 0
CUI: C1739147
Disease: Subacute necrotising encephalomyopathy
Subacute necrotising encephalomyopathy 		1 0 1 2.9E-02 0 0
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 2.9E-02 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 10 1 2.9E-02 1 7.7E-02
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 2.9E-02 0 0
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 2.9E-02 0 0
CUI: C1846171
Disease: Lissencephaly, X-Linked, 2
Lissencephaly, X-Linked, 2 		1 0 1 2.9E-02 0 0
CUI: C1846172
Disease: Hydranencephaly and Abnormal Genitalia
Hydranencephaly and Abnormal Genitalia 		1 0 1 2.9E-02 0 0
CUI: C1854685
Disease: Hypoplasia of the retina
Hypoplasia of the retina 		1 0 1 2.9E-02 0 0
CUI: C1855905
Disease: Microbrachycephaly
Microbrachycephaly 		1 1 1 2.9E-02 1 0.25
CUI: C1857813
Disease: Macular Degeneration, Age-Related, 7
Macular Degeneration, Age-Related, 7 		1 0 1 2.9E-02 0 0
CUI: C1857814
Disease: MACULAR DEGENERATION, AGE-RELATED, NEOVASCULAR TYPE, SUSCEPTIBILITY TO
MACULAR DEGENERATION, AGE-RELATED, NEOVASCULAR TYPE, SUSCEPTIBILITY TO 		1 0 1 2.9E-02 0 0
CUI: C2674766
Disease: Myokymia 1
Myokymia 1 		1 0 1 2.9E-02 0 0
CUI: C2677326
Disease: Epileptic Encephalopathy, Early Infantile, 4
Epileptic Encephalopathy, Early Infantile, 4 		1 0 1 2.9E-02 0 0
CUI: C2677903
Disease: Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia 		1 0 1 2.9E-02 0 0
CUI: C2750247
Disease: Polymicrogyria, Asymmetric
Polymicrogyria, Asymmetric 		1 0 1 2.9E-02 0 0
CUI: C2931111
Disease: Myopia, susceptibility to
Myopia, susceptibility to 		1 0 1 2.9E-02 0 0
CUI: C3150411
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 		1 0 1 2.9E-02 0 0