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: C1835698
Disease: Keratitis, hereditary
Keratitis, hereditary 		2 2 2 0.50 2 2.3E-02
CUI: C3805604
Disease: FOVEAL HYPOPLASIA 1
FOVEAL HYPOPLASIA 1 		2 4 2 0.50 3 3.4E-02
CUI: C4703595
Disease: Increased proinsulin:insulin ratio
Increased proinsulin:insulin ratio 		2 0 2 0.50 0 0
CUI: C0344543
Disease: Aniridia type 2
Aniridia type 2 		3 0 2 0.40 0 0
CUI: C1833797
Disease: Optic Nerve Hypoplasia, Bilateral
Optic Nerve Hypoplasia, Bilateral 		3 4 2 0.40 2 2.2E-02
CUI: C2931803
Disease: Deletion 11p13
Deletion 11p13 		3 0 2 0.40 0 0
CUI: C1832671
Disease: Dysfunction of lateral corticospinal tracts
Dysfunction of lateral corticospinal tracts 		4 0 2 0.33 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 0.25 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 0.25 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 0.25 0 0
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		6 17 2 0.25 1 9.7E-03
CUI: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar 		1 0 1 0.25 0 0
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		1 3 1 0.25 1 1.1E-02
CUI: C1860268
Disease: Gonadal tissue inappropriate for external genitalia or chromosomal sex
Gonadal tissue inappropriate for external genitalia or chromosomal sex 		1 0 1 0.25 0 0
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: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		1 9 1 0.25 1 1.1E-02
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 1 1 0.25 1 1.1E-02
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 1 1 0.25 1 1.1E-02
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: C4310841
Disease: ANTERIOR SEGMENT DYSGENESIS 5, PETERS ANOMALY SUBTYPE
ANTERIOR SEGMENT DYSGENESIS 5, PETERS ANOMALY SUBTYPE 		1 1 1 0.25 1 1.1E-02
CUI: C4310884
Disease: ANTERIOR SEGMENT DYSGENESIS 5, MULTIPLE SUBTYPES
ANTERIOR SEGMENT DYSGENESIS 5, MULTIPLE SUBTYPES 		1 0 1 0.25 0 0