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: 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
CUI: C4024758
Disease: Intraretinal exudate
Intraretinal exudate
1 0 1 0.17 0 0
CUI: C4024828
Disease: Fine, reticulate skin pigmentation
Fine, reticulate skin pigmentation
1 0 1 0.17 0 0
Abnormality of the femoral neck or head region
1 0 1 0.17 0 0
Visual acuity light perception with projection
1 0 1 0.17 0 0
CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2
1 0 1 0.17 0 0