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: C0344550
Disease: Congenital retinal fold
Congenital retinal fold
3 0 2 0.29 0 0
CUI: C0004608
Disease: Retinopathy background
Retinopathy background
4 0 2 0.25 0 0
CUI: C0154828
Disease: Traction detachment of retina
Traction detachment of retina
4 0 2 0.25 0 0
CUI: C4727832
Disease: Telomere Syndrome
Telomere Syndrome
5 0 2 0.22 0 0
CUI: C4072980
Disease: Exudative vitreoretinopathy
Exudative vitreoretinopathy
6 0 2 0.20 0 0
CUI: C0423431
Disease: Subretinal exudate
Subretinal exudate
1 0 1 0.17 0 0
CUI: C0432273
Disease: Worth disease
Worth disease
1 0 1 0.17 0 0
CUI: C1327916
Disease: REVESZ SYNDROME (disorder)
REVESZ SYNDROME (disorder)
1 0 1 0.17 0 0
Metacarpal diaphyseal endosteal sclerosis
1 0 1 0.17 0 0
Metatarsal diaphyseal endosteal sclerosis
1 0 1 0.17 0 0
CUI: C1842154
Disease: Sclerotic vertebral body
Sclerotic vertebral body
1 0 1 0.17 0 0
CUI: C1843323
Disease: Van Buchem disease type 2
Van Buchem disease type 2
1 0 1 0.17 0 0
CUI: C1843330
Disease: OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
1 0 1 0.17 0 0
Exudative Vitreoretinopathy, Familial, X-Linked Recessive
1 0 1 0.17 0 0
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1
1 0 1 0.17 0 0
CUI: C1866080
Disease: HIGH BONE MASS
HIGH BONE MASS
1 0 1 0.17 0 0
EXUDATIVE VITREORETINOPATHY 4 (disorder)
1 0 1 0.17 0 0
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3
1 0 1 0.17 0 0
Unilateral vertebral artery hypoplasia
1 0 1 0.17 0 0
CUI: C3554669
Disease: Clavicular sclerosis
Clavicular sclerosis
1 0 1 0.17 0 0
EXUDATIVE VITREORETINOPATHY, X-LINKED
1 0 1 0.17 0 0
EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL DOMINANT
1 0 1 0.17 0 0
EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL RECESSIVE
1 0 1 0.17 0 0
EXUDATIVE VITREORETINOPATHY 4, DIGENIC
1 0 1 0.17 0 0
CUI: C4017128
Disease: SPONDYLOCOSTAL DYSOSTOSIS 4
SPONDYLOCOSTAL DYSOSTOSIS 4
1 0 1 0.17 0 0