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 0.33 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 0.33 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 0.33 0 0
CUI: C1969032
Disease: Cataract, Autosomal Dominant, Multiple Types 1
Cataract, Autosomal Dominant, Multiple Types 1 		1 0 1 0.33 0 0
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly 		1 0 1 0.33 0 0
CUI: C2751320
Disease: Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay 		1 2 1 0.33 1 0.20
CUI: C2931644
Disease: O'Donnell Pappas syndrome
O'Donnell Pappas syndrome 		1 0 1 0.33 0 0
CUI: C3640024
Disease: Unilateral microphthalmos
Unilateral microphthalmos 		1 0 1 0.33 0 0
CUI: C3805349
Disease: CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY
CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY 		1 0 1 0.33 0 0
CUI: C4017065
Disease: Autosomal dominant keratitis
Autosomal dominant keratitis 		1 0 1 0.33 0 0
CUI: C4017066
Disease: ANIRIDIA, ATYPICAL
ANIRIDIA, ATYPICAL 		1 0 1 0.33 0 0
CUI: C4017067
Disease: FOVEAL HYPOPLASIA 1 WITH CATARACT
FOVEAL HYPOPLASIA 1 WITH CATARACT 		1 0 1 0.33 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 0.33 0 0
CUI: C4310841
Disease: ANTERIOR SEGMENT DYSGENESIS 5, PETERS ANOMALY SUBTYPE
ANTERIOR SEGMENT DYSGENESIS 5, PETERS ANOMALY SUBTYPE 		1 0 1 0.33 0 0
CUI: C4310884
Disease: ANTERIOR SEGMENT DYSGENESIS 5, MULTIPLE SUBTYPES
ANTERIOR SEGMENT DYSGENESIS 5, MULTIPLE SUBTYPES 		1 0 1 0.33 0 0
CUI: C1835698
Disease: Keratitis, hereditary
Keratitis, hereditary 		2 0 1 0.25 0 0
CUI: C1850993
Disease: Foveal Hypoplasia, Isolated
Foveal Hypoplasia, Isolated 		2 0 1 0.25 0 0
CUI: C3805604
Disease: FOVEAL HYPOPLASIA 1
FOVEAL HYPOPLASIA 1 		2 0 1 0.25 0 0
CUI: C3808115
Disease: CATARACT 12, MULTIPLE TYPES
CATARACT 12, MULTIPLE TYPES 		2 0 1 0.25 0 0
CUI: C4022524
Disease: Hypoplastic anterior commissure
Hypoplastic anterior commissure 		2 0 1 0.25 0 0
CUI: C4022653
Disease: Abnormal muscle fiber protein expression
Abnormal muscle fiber protein expression 		2 0 1 0.25 0 0
CUI: C4024811
Disease: Peripheral vitreous opacities
Peripheral vitreous opacities 		2 0 1 0.25 0 0
CUI: C4024960
Disease: Unilateral polymicrogyria
Unilateral polymicrogyria 		2 0 1 0.25 0 0
CUI: C4073008
Disease: Abnormal best corrected visual acuity test
Abnormal best corrected visual acuity test 		2 0 1 0.25 0 0
CUI: C4703595
Disease: Increased proinsulin:insulin ratio
Increased proinsulin:insulin ratio 		2 0 1 0.25 0 0