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 9.1E-02 0 0
CUI: C0154870
Disease: Focal chorioretinitis
Focal chorioretinitis 		1 0 1 9.1E-02 0 0
CUI: C0271086
Disease: Toxic maculopathy
Toxic maculopathy 		1 0 1 9.1E-02 0 0
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy 		1 0 1 9.1E-02 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 9.1E-02 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 9.1E-02 0 0
CUI: C1334557
Disease: Malignant Adult Brain Neoplasm
Malignant Adult Brain Neoplasm 		1 0 1 9.1E-02 0 0
CUI: C1513718
Disease: Mucin-Producing Intrahepatic Cholangiocarcinoma
Mucin-Producing Intrahepatic Cholangiocarcinoma 		1 0 1 9.1E-02 0 0
CUI: C1839928
Disease: IRIS HYPOPLASIA WITH GLAUCOMA
IRIS HYPOPLASIA WITH GLAUCOMA 		1 0 1 9.1E-02 0 0
CUI: C1851481
Disease: Erythrokeratodermia with ataxia
Erythrokeratodermia with ataxia 		1 0 1 9.1E-02 0 0
CUI: C1859194
Disease: GRISCELLI SYNDROME, TYPE 1
GRISCELLI SYNDROME, TYPE 1 		1 0 1 9.1E-02 0 0
CUI: C1860157
Disease: Elejalde Disease
Elejalde Disease 		1 0 1 9.1E-02 0 0
CUI: C1862373
Disease: Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities
Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities 		1 0 1 9.1E-02 0 0
CUI: C1866422
Disease: RETINITIS PIGMENTOSA 19
RETINITIS PIGMENTOSA 19 		1 0 1 9.1E-02 0 0
CUI: C1866560
Disease: IRIDOGONIODYSGENESIS, TYPE 1 (disorder)
IRIDOGONIODYSGENESIS, TYPE 1 (disorder) 		1 0 1 9.1E-02 0 0
CUI: C1970573
Disease: MACULAR DEGENERATION, AGE-RELATED, 2, SUSCEPTIBILITY TO
MACULAR DEGENERATION, AGE-RELATED, 2, SUSCEPTIBILITY TO 		1 0 1 9.1E-02 0 0
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly 		1 0 1 9.1E-02 0 0
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		1 0 1 9.1E-02 0 0
CUI: C2676042
Disease: Skin-Hair-Eye Pigmentation, Variation In, 4
Skin-Hair-Eye Pigmentation, Variation In, 4 		1 0 1 9.1E-02 0 0
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		1 0 1 9.1E-02 0 0
CUI: C2931644
Disease: O'Donnell Pappas syndrome
O'Donnell Pappas syndrome 		1 0 1 9.1E-02 0 0
CUI: C3280856
Disease: ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION
ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION 		1 0 1 9.1E-02 0 0
CUI: C3640024
Disease: Unilateral microphthalmos
Unilateral microphthalmos 		1 0 1 9.1E-02 0 0
CUI: C3805349
Disease: CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY
CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY 		1 0 1 9.1E-02 0 0
CUI: C3887633
Disease: Dandy-Walker Syndrome, Familial
Dandy-Walker Syndrome, Familial 		1 0 1 9.1E-02 0 0