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: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 0.25 0 0
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 0.25 0 0
CUI: C0270629
Disease: Epidural Abscess
Epidural Abscess 		1 0 1 0.25 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 0.25 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia 		1 0 1 0.25 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 0.25 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 0.25 0 0
CUI: C0741621
Disease: Brachial artery occlusion
Brachial artery occlusion 		1 0 1 0.25 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 0.25 0 0
CUI: C0810006
Disease: Acute cerebrovascular disease
Acute cerebrovascular disease 		1 0 1 0.25 0 0
CUI: C1303010
Disease: Mydriasis, Congenital
Mydriasis, Congenital 		1 0 1 0.25 0 0
CUI: C1847725
Disease: SPINOCEREBELLAR ATAXIA 15
SPINOCEREBELLAR ATAXIA 15 		1 3 1 0.25 1 6.7E-02
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly 		1 0 1 0.25 0 0
CUI: C2931644
Disease: O'Donnell Pappas syndrome
O'Donnell Pappas syndrome 		1 0 1 0.25 0 0
CUI: C3640024
Disease: Unilateral microphthalmos
Unilateral microphthalmos 		1 0 1 0.25 0 0
CUI: C3805349
Disease: CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY
CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY 		1 0 1 0.25 0 0
CUI: C4017065
Disease: Autosomal dominant keratitis
Autosomal dominant keratitis 		1 0 1 0.25 0 0
CUI: C4017066
Disease: ANIRIDIA, ATYPICAL
ANIRIDIA, ATYPICAL 		1 0 1 0.25 0 0
CUI: C4017067
Disease: FOVEAL HYPOPLASIA 1 WITH CATARACT
FOVEAL HYPOPLASIA 1 WITH CATARACT 		1 0 1 0.25 0 0
CUI: C4017657
Disease: FOVEAL HYPOPLASIA 1 WITH OR WITHOUT ANTERIOR SEGMENT ANOMALIES
FOVEAL HYPOPLASIA 1 WITH OR WITHOUT ANTERIOR SEGMENT ANOMALIES 		1 0 1 0.25 0 0
CUI: C4274322
Disease: Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 15/16 		1 0 1 0.25 0 0
CUI: C4310841
Disease: ANTERIOR SEGMENT DYSGENESIS 5, PETERS ANOMALY SUBTYPE
ANTERIOR SEGMENT DYSGENESIS 5, PETERS ANOMALY SUBTYPE 		1 0 1 0.25 0 0
CUI: C4310884
Disease: ANTERIOR SEGMENT DYSGENESIS 5, MULTIPLE SUBTYPES
ANTERIOR SEGMENT DYSGENESIS 5, MULTIPLE SUBTYPES 		1 0 1 0.25 0 0
CUI: C0003132
Disease: Anoxic Encephalopathy
Anoxic Encephalopathy 		2 0 1 0.20 0 0
CUI: C0158638
Disease: Congenital anomaly of cerebrovascular system
Congenital anomaly of cerebrovascular system 		2 0 1 0.20 0 0